ClearanceBrief
510(k) K914874 ยท KNW Instrument, Biopsy

MANAN PRO-MAG AUTOMATIC BIOPSY DEVICE

ApplicantManan Medical Products, Inc., Northbrook IL, US
DecisionSubstantially Equivalent, Feb 18, 1992
ReceivedOct 29, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914874

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.