ClearanceBrief
510(k) K092059 ยท KNW Instrument, Biopsy

RP CUTTING NEEDLE

ApplicantRiverpoint Medical, Portland OR, US
DecisionSubstantially Equivalent, Sep 24, 2009
ReceivedJul 7, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092059

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.