510(k) K920884 ยท DQX Wire, Guide, Catheter
GUIDEWIRES, VARIOUS TYPES
| Applicant | Acme-Monaco Corp., Crisfield MD, US |
| Decision | Substantially Equivalent, Aug 19, 1992 |
| Received | Jan 2, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920884
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.