510(k) K880761 ยท DQX Wire, Guide, Catheter
TAPER-22 STEERABLE GUIDEWIRE
| Applicant | Target Therapeutics, Los Angeles CA, US |
| Decision | Substantially Equivalent, Aug 19, 1988 |
| Received | Feb 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880761
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.