ClearanceBrief
510(k) K120440 ยท KNW Instrument, Biopsy

PRESTO BREAST BIOPSY DEVICE

ApplicantSontina Medical, LLC, San Francisco CA, US
DecisionSubstantially Equivalent, May 17, 2012
ReceivedFeb 13, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120440

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.