510(k) K020979 ยท GKP Instrument, Coagulation, Automated
SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL #CA-7000
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Jun 27, 2002 |
| Received | Mar 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020979
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.