ClearanceBrief
510(k) K864385 ยท FCW Light Source, Fiberoptic, Routine

LUXTEC LIGHT SOURCES

ApplicantLuxtec Corp., Sturbridge MA, US
DecisionSubstantially Equivalent, Jan 13, 1987
ReceivedNov 5, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864385

DateFirm and productCodeLinked 510(k)
Jun 6, 2007Vision Systems Group, A Div of Viking Systems
Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 and Boston Scientific Spyglass 300W Light Source (M00546190)
Terminated
KOGNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.