ClearanceBrief
510(k) K133702 ยท KNW Instrument, Biopsy

PRESTO BREAST BIOPSY DEVICE

ApplicantSontina Medical, LLC, San Francisco CA, US
DecisionSubstantially Equivalent, Feb 28, 2014
ReceivedDec 3, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K133702

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.