Corpak Co.
Mchenry, IL, US
Corpak Co. appears in FDA device records in Mchenry, IL. FDA records list 24 510(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
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Corpak Co. between 1981 and 1998. The busiest year on record is 1981, with 4. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 4 |
| 1982 | 4 |
| 1983 | 2 |
| 1984 | 3 |
| 1985 | 2 |
| 1988 | 1 |
| 1990 | 2 |
| 1994 | 1 |
| 1995 | 2 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K964514 | CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS | FKO | Substantially Equivalent | |
| K970178 | CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM | KNT | Substantially Equivalent | |
| K935512 | CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE | KNT | Substantially Equivalent | |
| K944750 | CORFLO 300 PUMP | FRN | Substantially Equivalent - Subject to Tracking & PMS | |
| K931921 | CORPAK GASTROSTOMY TUBE | KNT | Substantially Equivalent | |
| K932847 | CORPAK ENTERAL PUMP | FRN | Substantially Equivalent - Subject to Tracking Reg. | |
| K902949 | CORPAK GRASPING FORCEPS | OCZ | Substantially Equivalent | |
| K901501 | CORPAK GASTROSTOMY TUBE | KGC | Substantially Equivalent | |
| K882867 | CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE | KNT | Substantially Equivalent | |
| K853253 | CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI | KNT | Substantially Equivalent | |
| K852792 | CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW | KNT | Substantially Equivalent | |
| K842257 | CORPAK URINARY DRAINAGE BAG | KNX | Substantially Equivalent | |
| K841819 | CORPAK FOLEY CATH TRAY W/16FR. TEFLON | KOD | Substantially Equivalent | |
| K840292 | URETHRAL CATH. TRAY W/BAG | KNX | Substantially Equivalent | |
| K832167 | CORPAK VTR 300 ENTERNAL PUMP | FRN | Substantially Equivalent | |
| K830965 | ENTERAL SOLUTION ADMIN. PUMP SET | KNT | Substantially Equivalent | |
| K821410 | CORPAK-MONITOR ENTERAL FEEDING CONTAIN | KNT | Substantially Equivalent | |
| K821409 | CORPAK-ENTERAL FEEDING CONTAINER | KNT | Substantially Equivalent | |
| K820952 | OPTI-MIST | CAF | Substantially Equivalent | |
| K821036 | ENTERNAL SOLUTION ADMIN. SET | KNT | Substantially Equivalent | |
| K810559 | OPTI- SYSTEM | BTT | Substantially Equivalent | |
| K810219 | PREFILLED HUMIDIFER | BTT | Substantially Equivalent | |
| K810218 | PREFILLED NEBULIZER | CAF | Substantially Equivalent | |
| K810217 | NEBULIZER HEATER | CAF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- FKOCatheter, Peritoneal Dialysis, Single Use
- KODCatheter, Urological
- KNXCollector, Urine, (And Accessories) For Indwelling Catheter
- OCZEndoscopic Grasping/Cutting Instrument, Non-Powered
- BTTHumidifier, Respiratory Gas, (Direct Patient Interface)
- CAFNebulizer (Direct Patient Interface)
- FRNPump, Infusion
- KGCTube, Gastro-Enterostomy
- KNTTubes, Gastrointestinal (And Accessories)
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 Corpak Co. 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 Corpak Co.. 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