510(k) K953821 ยท DTN Reservoir, Blood, Cardiopulmonary Bypass
BIOCOR 200 HARDSHELL VENOUS RESERVIOR
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 7, 1996 |
| Received | Aug 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953821
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.