510(k) K960875 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
KC 40 MICRO COAGULATION ANALYZER SYSTEM (K3632)
| Applicant | Sigma Diagnostics, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Sep 10, 1996 |
| Received | Mar 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960875
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.