FDA 510(k) Applications for Medical Device Product Code "FQP"
(Lamp, Operating-Room)

FDA 510(k) Number Applicant Device Name Decision Date
K001223 ACULUX ACULUX, MODEL AX3001, AX3002 06/23/2000
K993314 SYNTHES (USA) SYNTHES LIGHT GUIDE 12/06/1999


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