510(k) K854938 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
COASCREENER/DIASCREENERBLOOD PLASMA TIMING INST.
| Applicant | Diatech, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Mar 12, 1986 |
| Received | Dec 10, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854938
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.