510(k) K961836 ยท DTN Reservoir, Blood, Cardiopulmonary Bypass
MAXIMA FORTE HARDSHELL VENOUS RESERVOIR
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Nov 1, 1996 |
| Received | May 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961836
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.