FDA 510(k) Applications Submitted by JAMES 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.