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. |
| K243540 |
11/15/2024 |
Mac-Lab (AltiX AI.i); CardioLab (AltiX AI.i); ComboLab (AltiX AI.i); MLCL Client Software (AltiX AI.i) |
GE Medical Systems Information Technologies, Inc. |
| 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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