510(k) K012050 ยท DQY Catheter, Percutaneous
VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 6, 2001 |
| Received | Jul 2, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012050
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.