ClearanceBrief
510(k) K080962 ยท FST Light, Surgical, Fiberoptic

LITE WAND II

ApplicantThompson Surgical Instruments, Inc., Traverse City MI, US
DecisionSubstantially Equivalent, Jun 25, 2008
ReceivedApr 4, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080962

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.