510(k) K950026 ยท DQY Catheter, Percutaneous
MEDTRONIC(R) 8.2 FRENCH SHERPA(R) SUPER PEAK FLOW(TM) CORONARY GUIDING CATHETER
| Applicant | Medtronics Interventional Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Apr 5, 1995 |
| Received | Jan 4, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950026
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.