ClearanceBrief
510(k) K201244 ยท KNW Instrument, Biopsy

Concorde Models Concorde US and Concorde ST Soft Tissue Biopsy Devices

ApplicantTransmed7, LLC, Portola Valley CA, US
DecisionSubstantially Equivalent, Aug 7, 2020
ReceivedMay 8, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201244

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.