510(k) K023362 ยท GKP Instrument, Coagulation, Automated
FISHER DIAGNOSTICS THROMBOSCREEN 1000; PACIFIC HEMOSTASIS FIBRINOGEN REAGENT PLUS KAOLIN
| Applicant | Fisher Diagnostics, Middletown VA, US |
| Decision | Substantially Equivalent, Dec 9, 2002 |
| Received | Oct 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023362
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.