ClearanceBrief
510(k) K883723 ยท DWZ Device, Biopsy, Endomyocardial

FLEXIBLE MYOCARDIAL BIOPSY FORCEPS

ApplicantCook, Inc., Bloomington IN, US
DecisionSubstantially Equivalent, Dec 5, 1988
ReceivedAug 31, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883723

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.