Gmdasz Manufacturing Co., Ltd. is one of 19001 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gmdasz Manufacturing Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Adhesive Electrodes, GMDASZ TENS ELECTRODES, MODELS CWN1005, DIA. 5CM, DWN2505, 5CMX5CM, CWN1007.DIA. 7CM, CWN2509,5CMX9CM
2
Total
2
Cleared
0
Denied
Gmdasz Manufacturing Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Echo, US.
Historical record: 2 cleared submissions from 2009 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Gmdasz Manufacturing Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Irc as regulatory consultant.
FDA 510(k) Regulatory Record - Gmdasz Manufacturing Co., Ltd.
2 devices