510(k) K990823 ยท DQX Wire, Guide, Catheter
PVS 1400 GUIDEWIRE
| Applicant | Precision Vascular Systems, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 23, 1999 |
| Received | Mar 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990823
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.