510(k) K930961 ยท DQX Wire, Guide, Catheter
CATHETER GUIDEWIRE (PERIPHERAL USE)
| Applicant | Target Therapeutics, Freemont CA, US |
| Decision | Substantially Equivalent, May 26, 1993 |
| Received | Feb 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930961
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.