510(k) K850542 ยท JCA Device, Bleeding Time
SURGICUTT - BLEEDING TIME DEVICE
| Applicant | International Technidyne Corp., Edison NJ, US |
| Decision | Substantially Equivalent, Mar 1, 1985 |
| Received | Feb 11, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850542
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.