Cure Medical, LLC is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cure Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: CURE CATHETER FEMALE, CURE CATHETER MALE, CURE CATHETER COUDE, CURE CATHETER PEDIATRIC, CURE CATHETER HYDROPHILIC COATED, CURE CATHETER, CURE CATHETER CLOSED SYSTEM
4
Total
4
Cleared
0
Denied
Cure Medical, LLC has 4 FDA 510(k) cleared medical devices. Based in Laguna Niguel, US.
Historical record: 4 cleared submissions from 2007 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cure Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cure Medical, LLC
4 devices
Cleared
Dec 23, 2013
CURE CATHETER FEMALE, CURE CATHETER MALE, CURE CATHETER COUDE, CURE CATHETER...
Gastroenterology & Urology
136d
Cleared
Aug 01, 2011
CURE CATHETER
Gastroenterology & Urology
147d
Cleared
Jun 11, 2008
CURE CATHETER CLOSED SYSTEM
Gastroenterology & Urology
72d
Cleared
Sep 13, 2007
CURE CATHETER
Gastroenterology & Urology
3d