510(k) K942117 ยท GKP Instrument, Coagulation, Automated
STA AUTOMATED MULTI-PARAMETRIC ANALYZER
| Applicant | American Bioproducts Co., Parisppany NJ, US |
| Decision | Substantially Equivalent, Feb 1, 1995 |
| Received | May 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942117
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.