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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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