510(k) K903923 ยท DQX Wire, Guide, Catheter
USCI(R) SILK (TM) GUIDE WIRE
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Nov 21, 1990 |
| Received | Aug 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903923
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.