FDA 510(k) Applications for Medical Device Product Code "IWE"
(Monitor, Patient Position, Light-Beam)

FDA 510(k) Number Applicant Device Name Decision Date
K152303 GAMMEX, INC. CT Sim Laser System 09/11/2015
K973162 HOGAN & HARTSON DUAL RADIATION TARGETING SYSTEM DRTS DRAPE 11/20/1997
K955236 MEDTEC, INC. GREEN TEC-2100 05/24/1996


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