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FDA 510(k) Applications Submitted by JAMES S TURNER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K092140
07/15/2009
GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
K082333
08/14/2008
ASAP WOUND DRESSING GEL
AMERICAN BIOTECH LABS
K092079
07/09/2009
MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
K213972
12/20/2021
Mac-Lab Recording Systems AltiX, CardioLab Recording Systems AltiX, ComboLab Recording Systems AltiX, MLCL Client Software AltiX
GE Healthcare Information Technologies, Inc.
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