510(k) K950179 ยท DQY Catheter, Percutaneous
MEDTRONIC(R) GC III CORONARY GUIDING CATHETER
| Applicant | Medtronics Interventional Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Jul 25, 1995 |
| Received | Jan 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950179
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.