ClearanceBrief
510(k) K252722 ยท DWZ Device, Biopsy, Endomyocardial

Biopsy Forceps

ApplicantFehling Instruments GmbH, Karlstein, DE
DecisionSubstantially Equivalent, Sep 30, 2025
ReceivedAug 28, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K252722

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.