ClearanceBrief
510(k) K913987 ยท ITY Assembly, Tube Housing, X-Ray, Diagnostic

OR340 INTRAOPERATIVE ULTRASOUND BIOPSY NEEDLE GUID

ApplicantCodman & Shurtleff, Inc., Randolph MA, US
DecisionSubstantially Equivalent, Apr 13, 1992
ReceivedSep 5, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913987

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.