ClearanceBrief
510(k) K893807 ยท KZF Device, Medical Examination, Ac Powered

MODEL 0183010, PEARL MEDICAL EXAM LIGHT

ApplicantBurton Medical Products Corp., Van Nuys CA, US
DecisionSubstantially Equivalent, Aug 15, 1989
ReceivedMay 22, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893807

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.