Hospal Medical Corp.
Mchenry, IL, US
Hospal Medical Corp. appears in FDA device records in Mchenry, IL. FDA records list 55 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 55
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
Showing 50 of 55FDA records hold 55 510(k) clearances for Hospal Medical Corp. between 1977 and 1989. The busiest year on record is 1984, with 8. The most recent is 1989, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 2 |
| 1978 | 6 |
| 1979 | 5 |
| 1980 | 3 |
| 1981 | 1 |
| 1982 | 5 |
| 1983 | 7 |
| 1984 | 8 |
| 1985 | 7 |
| 1986 | 5 |
| 1987 | 2 |
| 1988 | 3 |
| 1989 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K893742 | FILTRAL TM 20 HEMODIALYZER/FILTER | KDI | Substantially Equivalent | |
| K884365 | MULTIFLOW(TM) 60 KIT | KDI | Substantially Equivalent | |
| K884326 | FILTRAL TM 8 HEMODIALYZER | KDI | Substantially Equivalent | |
| K883307 | CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT | KDI | Substantially Equivalent | |
| K872767 | FILTRAL 10, FILTRAL 12, FILTRAL 16 HEMODIALYZER | KDI | Substantially Equivalent | |
| K871218 | MONITRAL S GS HEMODIALYSIS SINGLE PATIENT UNIT | FKP | Substantially Equivalent | |
| K863961 | HOSPAL BIOSPAL 1800S | KDI | Substantially Equivalent | |
| K863592 | DISSCAP 80E, 110E, 140E, 160E | FJI | Substantially Equivalent | |
| K861156 | HOSPAL DIALYSATE FOR CAVHD | KPO | Substantially Equivalent | |
| K861230 | MONITRAL S | FKP | Substantially Equivalent | |
| K854951 | PLUME Y SET | FIE | Substantially Equivalent | |
| K852885 | FILTRAL HEMODIALYZER | KDI | Substantially Equivalent | |
| K852135 | BSM 21 BLOOD SAFETY MODULE | KOC | Substantially Equivalent | |
| K852134 | BSM 22 BLOOD SAFETY MODULE | KOC | Substantially Equivalent | |
| K852073 | VIAL SYRINGE PUMPS, SE200, SE200B & SE400 | FRN | Substantially Equivalent | |
| K851453 | HOSPAL FISTULA NEEDLE | FIE | Substantially Equivalent | |
| K851380 | DISSCAP 110 DIALYZER | FJI | Substantially Equivalent | |
| K850179 | MBM(TM) MONITRAL (R) BICARBONATE MODULE | FKP | Substantially Equivalent | |
| K841791 | PLUME FISTULA NEEDLE | FIQ | Substantially Equivalent | |
| K841152 | HOSPAL BIOSPAL SCU/CAVH KIT | KDI | Substantially Equivalent | |
| K840814 | HOSPAL MODEL H1210 | FKQ | Substantially Equivalent | |
| K840813 | BIOSPAL 1200S | FKQ | Substantially Equivalent | |
| K840812 | BIOSPAL 2400S | FKQ | Substantially Equivalent | |
| K840811 | BIOSPAL 3000S | FKQ | Substantially Equivalent | |
| K834589 | BIOSPAL (R) 1800S | KDI | Substantially Equivalent | |
| K834579 | BIOSPAL 2400S | KDT | Substantially Equivalent | |
| K833440 | BLOOD SAFETY MODULE BSM2 | KOC | Substantially Equivalent | |
| K832659 | BIOSPAL 1200S | KDI | Substantially Equivalent | |
| K832645 | BIOSPAL 3000 S | KDI | Substantially Equivalent | |
| K830595 | MONITRAL | KDI | Substantially Equivalent | |
| K830648 | H1207 | KDI | Substantially Equivalent | |
| K830647 | H1210 | KDI | Substantially Equivalent | |
| K823707 | HOSPAL BLOOD LINES | KOC | Substantially Equivalent | |
| K823589 | H 12 07 | KDI | Substantially Equivalent | |
| K822386 | COTRAL I W/4.5 L/HR. ULTRAFILTRAT. CAPA | FII | Substantially Equivalent | |
| K822851 | DISSCAP 080 | FKQ | Substantially Equivalent | |
| K820966 | DISSCAP 110 | FKQ | Substantially Equivalent | |
| K820965 | DISSCAP 140 | FKQ | Substantially Equivalent | |
| K812575 | MODEL H12-10 | KDI | Substantially Equivalent | |
| K802466 | DISSCAP HOLLOW FIBER DIALYZER | FJI | Substantially Equivalent | |
| K800536 | MODEL H 607-.67M2 30 MICRON RP AN69 MEM | KDI | Substantially Equivalent | |
| K800650 | MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM | CBK | Substantially Equivalent | |
| K791490 | UNIPUNCTURE CATHETER | FIE | Substantially Equivalent | |
| K791489 | VITAL CATHETER | FIE | Substantially Equivalent | |
| K790827 | RP-610 PARALLEL PLATE DIALYZER | KDI | Substantially Equivalent | |
| K791448 | HEMODIALYZERS RP-510 AND RP-514 | FJG | Substantially Equivalent | |
| K790001 | DIALYZER, MODEL F.M.D 150 | FJG | Substantially Equivalent | |
| K781464 | HEMODIALYZER, MODEL RP610, RP AN 69 | KDI | Substantially Equivalent | |
| K780527 | CORTRAL I | KDI | Substantially Equivalent | |
| K781142 | DISSCAP | FJI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KOCAccessories, Blood Circuit, Hemodialysis
- BZCCalculator, Pulmonary Function Data
- FIQCannula, A-V Shunt
- KDTContainer, Specimen Mailer And Storage, Sterile
- FJFDetector, Air Bubble
- KPODialysate Concentrate For Hemodialysis (Liquid Or Powder)
- FJIDialyzer, Capillary, Hollow Fiber
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- FJGDialyzer, Parallel Flow
- CAFNebulizer (Direct Patient Interface)
- FIENeedle, Fistula
- FRNPump, Infusion
- FKQSystem, Dialysate Delivery, Central Multiple Patient
- FIISystem, Dialysate Delivery, Sealed
- FKPSystem, Dialysate Delivery, Single Patient
- CBKVentilator, Continuous, Facility Use
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Hospal Medical Corp. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Hospal Medical Corp.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain
