510(k) K955724 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
KC 1A COAGULATION ANALYZER/SET
| Applicant | Sigma Diagnostics, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 12, 1996 |
| Received | Dec 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955724
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.