510(k) K874771 ยท DWB Pump, Blood, Cardiopulmonary Bypass, Roller Type
ANGIOMED INTRODUCING SETS
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Jan 12, 1988 |
| Received | Nov 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874771
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.