510(k) K883579 ยท DQX Wire, Guide, Catheter
CORONARY GUIDE WIRE
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Nov 4, 1988 |
| Received | Aug 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883579
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.