ClearanceBrief
510(k) K032847 ยท KNW Instrument, Biopsy

EXCISOR BIOPTOME, MODEL 01-0004

ApplicantAcueity, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Sep 26, 2003
ReceivedSep 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032847

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.