Delta Medical Industries
Mchenry, IL, US
Delta Medical Industries appears in FDA device records in Mchenry, IL. FDA records list 27 510(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
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Delta Medical Industries between 1976 and 1984. The busiest year on record is 1980, with 5. The most recent is 1984, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 2 |
| 1977 | 3 |
| 1978 | 3 |
| 1979 | 4 |
| 1980 | 5 |
| 1981 | 2 |
| 1982 | 3 |
| 1983 | 2 |
| 1984 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K833884 | ISOTEC DISPOS. PRESSURE TRANSDUCER | Substantially Equivalent | ||
| K840253 | ONE-WAY AIR VALVE | BYZ | Substantially Equivalent | |
| K832470 | INFUSION PUMP | FRN | Substantially Equivalent | |
| K830389 | ACCU-RYNGE PUMP SP-250 | FRN | Substantially Equivalent | |
| K831750 | PM-3 | DXS | Substantially Equivalent | |
| K822761 | DELIVERY TUBE SET #2226 | FRN | Substantially Equivalent | |
| K820912 | PMS-2 PRESSURE MONITOR SEPARATOR | DXS | Substantially Equivalent | |
| K820482 | ACCU-RYNGE INSULIN PUMP #SP-250 | FRN | Substantially Equivalent | |
| K810068 | PEDIATRIC ARTERIAL BLOOD FILTER | DTM | Substantially Equivalent | |
| K802755 | ARTERIAL BLOOD FILTER BF-37 | DTM | Substantially Equivalent | |
| K803102 | ARTERIAL BUBBLE TRAP K-20 | KRL | Substantially Equivalent | |
| K803101 | PREBYPASS FILTER CAT.#K-5 | KRJ | Substantially Equivalent | |
| K802602 | L-3 PURGE LINE | DTM | Substantially Equivalent | |
| K801704 | OPEN-LOOP INSULIN DELIVERY SYSTEM | FRN | Substantially Equivalent | |
| K801770 | ARTERIAL BUBBLE TRAP | DWF | Substantially Equivalent | |
| K792182 | ICE CONTAINER I.C.E. | IME | Substantially Equivalent | |
| K790406 | DELTA D-750 THERMAFLOW | DTZ | Substantially Equivalent | |
| K790756 | HEAT EXCHANGER COIL | DTR | Substantially Equivalent | |
| K790116 | CARDIOTOMY RESERVOIR CR-2000 | DTB | Substantially Equivalent | |
| K781890 | CHAMBER, MC-1 DISPOSABLE PRESSURE | DXS | Substantially Equivalent | |
| K781210 | HEAT EXCHANGER, FHX-14 | DTR | Substantially Equivalent | |
| K780485 | PREBYPASS FILTER | KRJ | Substantially Equivalent | |
| K771014 | TS-100 TEST SYSTEM | KRC | Substantially Equivalent | |
| K770344 | SH-1 | CBN | Substantially Equivalent | |
| K770546 | BLOOD RESERVOIR | DTN | Substantially Equivalent | |
| K760895 | AUTOMATIC SHUT-OFF VALVE | KZD | Substantially Equivalent | |
| K760894 | VACUUM RELIEF VALVE | DWD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CBNApparatus, Gas-Scavenging
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- KRLDetector, Bubble, Cardiopulmonary Bypass
- DTMFilter, Blood, Cardiopulmonary Bypass, Arterial Line
- KRJFilter, Prebypass, Cardiopulmonary Bypass
- DXSGauge, Pressure, Coronary, Cardiopulmonary Bypass
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- KZDInfusor, Pressure, For I.V. Bags
- DTZOxygenator, Cardiopulmonary Bypass
- IMEPack, Hot Or Cold, Reusable
- DTBPermanent Pacemaker Electrode
- FRNPump, Infusion
- DTNReservoir, Blood, Cardiopulmonary Bypass
- DWDSuction Control, Intracardiac, Cardiopulmonary Bypass
- KRCTester, Electrode, Surface, Electrocardiographic
- BYZTrap, Sterile Specimen
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain