ClearanceBrief
510(k) K931956 ยท GKP Instrument, Coagulation, Automated

CASCADE M, CAT. NO. 1710

ApplicantHelena Laboratories, Beaumont TX, US
DecisionSubstantially Equivalent, Aug 23, 1993
ReceivedApr 20, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931956

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.