ClearanceBrief
510(k) K024089 ยท KNW Instrument, Biopsy

VACUFLASH BIOPSY SYSTEM

ApplicantBip USA, Inc., Niagara Falls NY, US
DecisionSubstantially Equivalent, Mar 11, 2003
ReceivedDec 11, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K024089

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.