510(k) K934433 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
VANTAGE DIALTAION CATHETER
| Applicant | Peripheral Systems Group, Mountain View CA, US |
| Decision | Substantially Equivalent, Dec 9, 1993 |
| Received | Sep 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934433
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.