510(k) K901380 ยท GKP Instrument, Coagulation, Automated
CASCADE 480(TM) AUTOMATED COAGULATION ANALY. 1430
| Applicant | Helena Laboratories, Beaumont TX, US |
| Decision | Substantially Equivalent, May 25, 1990 |
| Received | Mar 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901380
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.