3M Company
Ann Arbor, MI, US
3M Company appears in FDA device records in Ann Arbor, MI. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for 3M Company between 1989 and 1990. The busiest year on record is 1990, with 7. The most recent is 1990, with 7.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 6 |
| 1990 | 7 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K902404 | SARNS DELPHIN CENTRIFUGAL SYSTEM W/DIRECTION. FLOW | KFM | Substantially Equivalent | |
| K902198 | SARNS DELPHIN BASE ADAPTER WITH BATTERY | KFM | Substantially Equivalent | |
| K900815 | SARNS 9000 PERFUSION SYSTEM W/ALERT ONLY LEVEL | DTW | Substantially Equivalent | |
| K900640 | MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU | DTR | Substantially Equivalent | |
| K900601 | SARNS DELPHIN BASE ADAPTER WITH MINI-BATTERY | KFM | Substantially Equivalent | |
| K897039 | SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM) | DTR | Substantially Equivalent | |
| K896671 | SARNS MEMBRANE OXYGENATOR W/INTEGRAL RESER. #9461 | DTZ | Substantially Equivalent | |
| K895632 | SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380 | DTZ | Substantially Equivalent | |
| K895393 | SARNS INGANT MEMBRANE OXYGENATOR | DTZ | Substantially Equivalent | |
| K893683 | SARNS PRESSURE ADJUSTABLE SAFETY SYSTEM | DTL | Substantially Equivalent | |
| K892052 | SARNS MEDICAL CART | LDQ | Substantially Equivalent | |
| K890808 | SARNS MEMBRANE OXYGENATOR W/INTEGRAL CARDIO RESERV | DTZ | Substantially Equivalent | |
| K890024 | SARNS VENT CATHETER | DWF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- DTWMonitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
- DTZOxygenator, Cardiopulmonary Bypass
- KFMPump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain