ClearanceBrief
510(k) K912905 ยท CCW Laryngoscope, Rigid

LARYNGOSCOPE

ApplicantAcorn Group, Inc., Walnut Creek CA, US
DecisionSubstantially Equivalent, Sep 30, 1991
ReceivedJul 2, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912905

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.