ClearanceBrief
510(k) K925875 ยท GDF Guide, Needle, Surgical

HORIZONTAL NEEDLE GUIDE ATTACHMENT

ApplicantBip USA, Inc., Niagara Falls NY, US
DecisionSubstantially Equivalent, Apr 6, 1993
ReceivedNov 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925875

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.