510(k) K901347 ยท DQX Wire, Guide, Catheter
DATASCOPE SLIDEWIRE(TM)
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Jun 21, 1990 |
| Received | Mar 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901347
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.