ClearanceBrief
510(k) K921401 ยท DWZ Device, Biopsy, Endomyocardial

BIOPSY FORCEPS

ApplicantAnnex Medical, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Oct 21, 1992
ReceivedMar 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921401

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.