ClearanceBrief
510(k) K920103 ยท KZF Device, Medical Examination, Ac Powered

EPISCOPE, MODEL 47300

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Apr 28, 1992
ReceivedJan 9, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920103

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.