510(k) K991194 ยท DQX Wire, Guide, Catheter
MODIFICATION TO ULTRA-SELECT GUIDEWIRE
| Applicant | Microvena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, May 5, 1999 |
| Received | Apr 8, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991194
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.