ClearanceBrief
510(k) K894765 ยท FYD Apparatus, Exhaust, Surgical

SHARPLAN SMOKE EVACUATION UNIT, MODEL 100

ApplicantLaser Industries , Ltd., Allendale NJ, US
DecisionSubstantially Equivalent, Sep 28, 1989
ReceivedJul 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894765

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.