FDA 510(k) Applications Submitted by GE MEDICAL SYSTEMS CHINA CO., LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K130584 |
03/05/2013 |
MONITOR B40 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K103633 |
12/13/2010 |
ACHILLES |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K123238 |
10/16/2012 |
ACHILLES |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K120598 |
02/28/2012 |
PROCARE MONITOR B40 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K122253 |
07/27/2012 |
PROCARE MONITOR B20 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K133576 |
11/20/2013 |
MONITOR B40 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K151063 |
04/20/2015 |
Monitor B40 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K142288 |
08/18/2014 |
MAC 800 Resting ECG Analysis System |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K091164 |
04/22/2009 |
GE VENUE 40, MODEL 5324338 |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K091374 |
05/11/2009 |
GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K102113 |
07/28/2010 |
GE VENUE 40 COMPACT DIAGNOSTIC ULTRASOUND |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
| K102256 |
08/10/2010 |
GE LOGIQ I/E & VIVID E COMPACT DIAGNOSTIC ULTRASOUND |
GE MEDICAL SYSTEMS CHINA CO., LTD. |
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