ClearanceBrief
510(k) K222462 ยท KNW Instrument, Biopsy

Semi-automatic Biopsy-Needle (BIM 18/20); Semi-automatic Biopsy-Needle (BIM 18.15); Semi-automatic Biopsy-Needle (BIM 18/10);Semi-automatic Biopsy-Needle (BIM 16/20);Semi-automatic Biopsy-Needle (BIM 16/15);Semi-automatic Biopsy-Needle (BIM 16/10);Semi-automatic Biopsy-Needle (BIM 14/20);Semi-automa

ApplicantItp Innovative Tomography Products GmbH, Bochum, DE
DecisionSubstantially Equivalent, Jan 20, 2023
ReceivedAug 15, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222462

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.