ClearanceBrief
510(k) K901302 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BIPOLARD POLYPECTOMY SYSTEM (TM)

ApplicantMedical Devices, Inc., Hackensack NJ, US
DecisionSubstantially Equivalent, Jun 6, 1990
ReceivedMar 20, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901302

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.