ClearanceBrief
510(k) K842975 ยท FTC Light, Ultraviolet, Dermatological

BROWNIE BOOTH BB1

ApplicantWeingart, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 17, 1984
ReceivedJul 30, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842975

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.