510(k) K955554 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
HEMO-VALVE
| Applicant | North American Instrument Corp., Glens Falls NY, US |
| Decision | Substantially Equivalent, Mar 4, 1996 |
| Received | Dec 5, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955554
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.