ClearanceBrief
510(k) K820492 ยท FTC Light, Ultraviolet, Dermatological

SPECTRA305

ApplicantUltralite, Walker MI, US
DecisionSubstantially Equivalent, Mar 31, 1982
ReceivedFeb 23, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820492

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.