510(k) K981711 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
SYSMEX AUTOMATED COAGULATION ANALYZER CA-500
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Sep 30, 1998 |
| Received | Apr 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981711
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.