510(k) K960755 ยท DQX Wire, Guide, Catheter
CARDIOTHERM BLOOD CARDIOPLEGIA SYSTEMS
| Applicant | Medtronic Cardiac Surgery, Medtronic, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, May 23, 1996 |
| Received | Feb 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960755
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.