ClearanceBrief
510(k) K926559 ยท FCG Biopsy Needle

PROACT BIOPSY NEEDLE ENCHANCEMENTS

ApplicantProact, Ltd., State College PA, US
DecisionSubstantially Equivalent, Mar 22, 1993
ReceivedDec 31, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926559

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.