ClearanceBrief
510(k) K950810 ยท FCG Biopsy Needle

RUTNER BIOPSY DEVICE

ApplicantCook Urological, Inc., Spencer IN, US
DecisionSubstantially Equivalent, Mar 6, 1995
ReceivedFeb 22, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950810

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.