510(k) K760594 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
AUTO-FI COAGULATION INSTRUMENT
| Applicant | Dade, Baxter Travenol Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 24, 1976 |
| Received | Sep 7, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760594
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.