510(k) K992321 ยท GKP Instrument, Coagulation, Automated
SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000
| Applicant | Dade Behring, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Sep 17, 1999 |
| Received | Jul 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992321
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.