ClearanceBrief
510(k) K810796 ยท FTC Light, Ultraviolet, Dermatological

SUNTAN BOOTH

ApplicantGibson'S Mfg. Corp., Walker MI, US
DecisionSubstantially Equivalent, Aug 3, 1981
ReceivedMar 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810796

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.