ClearanceBrief
510(k) K894949 ยท POV Semen Analysis Device

SQA

ApplicantUnited Medical Systems, Inc., Washington DC, US
DecisionSubstantially Equivalent, Dec 29, 1989
ReceivedAug 3, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894949

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.