ClearanceBrief
510(k) K883573 ยท FLK Thermometer, Clinical Mercury

THERMOMETER, MERCURY/CLINICAL

ApplicantUmax Corp., West Hartford CT, US
DecisionSubstantially Equivalent, Nov 7, 1988
ReceivedAug 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883573

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.