ClearanceBrief
510(k) K935832 ยท KZF Device, Medical Examination, Ac Powered

CHROMOPHARE

ApplicantBerchtold Holding GmbH, Tuttlingen, DE
DecisionSubstantially Equivalent, Feb 3, 1994
ReceivedDec 7, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935832

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.