510(k) K851613 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
CENTRIMED SYSTEM 1 W/SYSTEM 1 ADAPTER
| Applicant | Centrimed Corp., Hopkins MN, US |
| Decision | Substantially Equivalent, Jun 19, 1985 |
| Received | Apr 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851613
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.