ClearanceBrief
510(k) K103375 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

PLUMEPEN INTEGRATED SMOKE EVACUATION PENCIL

ApplicantMedtek Devices, Inc., Buffalo NY, US
DecisionSubstantially Equivalent, Mar 16, 2011
ReceivedNov 16, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103375

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.