ClearanceBrief
510(k) K093386 ยท FST Light, Surgical, Fiberoptic

CHROMALUME TURBO LIGHT SOURCE WITH XTREMEBEAM FIBER OPTIC HEADLAMPFST MODEL FST

ApplicantBfw, Inc., Louisville KY, US
DecisionSubstantially Equivalent, Jan 28, 2010
ReceivedOct 30, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093386

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.