510(k) K965183 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
VANTAGE PERIPHERAL DILATATION CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Apr 24, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965183
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.