510(k) K911996 ยท JCA Device, Bleeding Time
SURGICUTT-BLEEDING TIME DEVICE, MODIFICATION
| Applicant | International Technidyne Corp., Edison NJ, US |
| Decision | Substantially Equivalent, Jul 17, 1991 |
| Received | Apr 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911996
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.