510(k) K881780 ยท DWB Pump, Blood, Cardiopulmonary Bypass, Roller Type
VASCUCARE ANGIOPUMP
| Applicant | Vascucare, Inc., Orangeburg NY, US |
| Decision | Substantially Equivalent, Sep 28, 1988 |
| Received | Apr 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881780
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.