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FDA 510(k) Applications Submitted by CORRINE MCLEOD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081022
04/10/2008
SOMATOM DEFINITION, MODEL AS/AS+
SIEMENS MEDICAL SOLUTIONS USA, INC.
K082220
08/06/2008
SOMATOM FLASH DS
SIEMENS MEDICAL SOLUTIONS USA INC.
K073003
10/24/2007
SYNGO DUAL ENERGY WITH EXTENDED FUNCTIONALLY
SIEMENS MEDICAL SOLUTIONS, INC.
K083524
11/28/2008
SYNGO DUAL ENERGY WITH EXTENDED FUNATIONALLY
SIEMENS MEDICAL SOLUTIONS USA, INC.
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