510(k) K983055 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Dec 30, 1998 |
| Received | Sep 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983055
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.