ClearanceBrief
510(k) K860489 ยท FTC Light, Ultraviolet, Dermatological

EUROTAN BY AYK

ApplicantEurotan Intl., Houston TX, US
DecisionSubstantially Equivalent for Some Indications, Feb 24, 1986
ReceivedFeb 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860489

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.