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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 88 Results
ProductCode: JAK Applicant: GE MEDICAL SYSTEMS Decision Date To: 02/23/2017
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revolution ct, revolution ct es, revolution apex, revolution ct with apex edition GE Medical Systems, LLC K191777 07/26/2019
revolution ct GE Medical Systems, L.L.C. K163213 12/16/2016
revolution ct GE MEDICAL SYSTEMS, LLC K133705 04/11/2014
revolution apex, revolution apex elite, revolution apex plus, revolution apex select,revolution ct; revolution ct es; revolution ct with apex edition; revolution ct es with apex edition GE Medical Systems,LLC K213715 12/17/2021
optima ct660 GE MEDICAL SYSTEMS, LLC K110227 07/20/2011
optima ct660 GE MEDICAL SYSTEMS, LLC K131576 08/30/2013
modification to: lightspeed plus mobile ct system GE MEDICAL SYSTEMS K012836 09/07/2001
modification to ge discovery ls system GE MEDICAL SYSTEMS K040172 04/07/2004
mobile ct prospeed family GE MEDICAL SYSTEMS K963896 12/18/1996
maxfov 2 GE Medical Systems, LLC. K203617 03/02/2021
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