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FDA 510(k) Applications Submitted by ANDREW MENDEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081105
04/18/2008
GE LIGHTSPEED CT750 HD (LIGHTSPEED 8.0)
GE HEALTHCARE
K202966
09/30/2020
SIGNA Architect
GE Healthcare (GE Medical Systems, LLC)
K153003
10/13/2015
SIGNA Pioneer
GE HEALTHCARE
K123327
10/26/2012
1.5T GEM RT OPEN ARRAY
GE HEALTHCARE COILS (USA INSTRUMENTS INC.)
K103489
11/26/2010
GE VEO RECONSTRUCTION OPTION
GENERAL ELECTRIC CO.
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