ClearanceBrief
510(k) K902614 ยท KQG Instrument, Coagulation

ELVI 828 DIGICLOT MULTISCAN

ApplicantLogos Scientific, Inc., Henderson NV, US
DecisionSubstantially Equivalent, Nov 8, 1990
ReceivedJun 13, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902614

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.