ClearanceBrief
510(k) K801017 ยท FTC Light, Ultraviolet, Dermatological

TANIT COMMERCIAL SUNTAN BOOTH

ApplicantTanit, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 17, 1980
ReceivedApr 30, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801017

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.