ClearanceBrief
510(k) K980122 ยท KNW Instrument, Biopsy

MANAN SOFT TISSUE BIOPSY NEEDLES

ApplicantMedical Device Technologies, Inc., Gainsville FL, US
DecisionSubstantially Equivalent, Jan 30, 1998
ReceivedJan 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980122

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.