510(k) K873543 ยท DQX Wire, Guide, Catheter
STUBBIE STEERABLE GUIDEWIRE
| Applicant | Target Therapeutics, Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 3, 1987 |
| Received | Sep 1, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873543
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.