Foshan Gaunying Electronics Co., Ltd. is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Foshan Gaunying Electronics Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ULTRASONIC MESH NEBULIZER, ULTRASONIC MESH NEBULIZER, ULTRASONIC NEBULIZER
6
Total
6
Cleared
0
Denied
Foshan Gaunying Electronics Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Historical record: 6 cleared submissions from 2010 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Foshan Gaunying Electronics Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Foshan Gaunying Electronics Co., Ltd.
6 devices
Cleared
May 30, 2014
ULTRASONIC MESH NEBULIZER
Anesthesiology
122d
Cleared
Jan 08, 2014
ULTRASONIC MESH NEBULIZER
Anesthesiology
173d
Cleared
Aug 20, 2012
ULTRASONIC NEBULIZER
Anesthesiology
126d
Cleared
Mar 30, 2011
GAUNYING INFRARED LAMP
Physical Medicine
15d
Cleared
Jan 05, 2011
GAUNYING INFRARED LAMP MODEL IL50
Physical Medicine
203d
Cleared
Aug 13, 2010
GAUNYING INFRARED LAMP
Physical Medicine
14d