ClearanceBrief
510(k) K111049 ยท FTC Light, Ultraviolet, Dermatological

MOBILE VERSA LIGHT

ApplicantMedtek Lighting Corp, Knoxville TN, US
DecisionSubstantially Equivalent, May 25, 2012
ReceivedApr 15, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111049

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.