ClearanceBrief
510(k) K183146 ยท KNW Instrument, Biopsy

Ranfac Cartilage Biopsy Needle

ApplicantRanfac Corporation, Avon MA, US
DecisionSubstantially Equivalent, Apr 25, 2019
ReceivedNov 13, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183146

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.