ClearanceBrief
510(k) K895098 ยท DWZ Device, Biopsy, Endomyocardial

BIOPSY FORCEPS

ApplicantAnnex Medical, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Oct 30, 1989
ReceivedAug 15, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895098

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.