510(k) K871318 ยท JCA Device, Bleeding Time
Q.I.C. BLEEDING TIME DEVICE
| Applicant | Helena Laboratories, Beaumont TX, US |
| Decision | Substantially Equivalent, Jun 10, 1987 |
| Received | Apr 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871318
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.