ClearanceBrief
510(k) K980004 ยท KNW Instrument, Biopsy

MANAN GENERAL PURPOSE INTRODUCER NEEDLE

ApplicantMedical Device Technologies, Inc., Gainsville FL, US
DecisionSubstantially Equivalent, Jan 9, 1998
ReceivedJan 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980004

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.