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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