ClearanceBrief
510(k) K863937 ยท FTC Light, Ultraviolet, Dermatological

OSRAM ULTRAMED 400 W

ApplicantOsram GmbH, West Germany, DE
DecisionSubstantially Equivalent for Some Indications, Nov 4, 1986
ReceivedOct 9, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863937

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.