510(k) K890800 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ROTATING HEMOSTATIC VALVE
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Jun 12, 1989 |
| Received | Feb 16, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890800
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.