ClearanceBrief
510(k) K925392 ยท FCL Forceps, Biopsy, Non-Electric

BIOPSY FORCEPS

ApplicantEndo-Therapeutics, Inc., Safety Harbor FL, US
DecisionSubstantially Equivalent, Nov 5, 1993
ReceivedOct 26, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925392

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.