ClearanceBrief
510(k) K852355 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SINGLE USE ARTHROSCOPY ELECTRODE

ApplicantAspen Laboratories, Inc., Englewood CO, US
DecisionSubstantially Equivalent, Sep 3, 1985
ReceivedJun 3, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852355

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.