ClearanceBrief
510(k) K993936 ยท KNW Instrument, Biopsy

15MM SITESELECT BREAST BIOPSY DEVICE, 10 MM SITESELECT BREAST BIOPSY DEVICE, 5MM SITESELECT BREAST BIOPSY DEVICE

ApplicantImagyn Surgical, Richland MI, US
DecisionSubstantially Equivalent, Dec 27, 1999
ReceivedNov 19, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993936

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.