510(k) K993639 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
RX VIATRAC 18 PERIPHERAL DILATATION CATHETER, OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jan 27, 2000 |
| Received | Oct 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993639
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.