ClearanceBrief
510(k) K003297 ยท KNW Instrument, Biopsy

MAMMOTOME HAND HELD PROBE, MODEL MHH8

ApplicantEthicon Endo-Surgery, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Jan 18, 2001
ReceivedOct 20, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003297

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.