ClearanceBrief
510(k) K011575 ยท KNW Instrument, Biopsy

22MM SITESELECT BREAST BIOPSY DEVICE MODEL SSD022

ApplicantImagyn Surgical, Richland MI, US
DecisionSubstantially Equivalent, Aug 17, 2001
ReceivedMay 22, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011575

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.