ClearanceBrief
510(k) K851831 ยท KNW Instrument, Biopsy

MANAN FRANSEENE NEEDLE

ApplicantManan Manufacturing Co., Inc., Skokie IL, US
DecisionSubstantially Equivalent, May 14, 1985
ReceivedApr 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851831

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.