ClearanceBrief
510(k) K071048 ยท KNW Instrument, Biopsy

RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537

ApplicantRubicor Medical, Inc., San Carlos CA, US
DecisionSubstantially Equivalent, May 15, 2007
ReceivedApr 13, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071048

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.