Mayer Laboratories, Inc. is one of 5184 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mayer Laboratories, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Mayer Laboratories, Inc. has 3 FDA 510(k) cleared medical devices. Based in Berkely, US.
Historical record: 3 cleared submissions from 2011 to 2013. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Mayer Laboratories, Inc. Filter by specialty or product code using the sidebar.
Mayer Laboratories, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Aug 01, 2013
AQUA LUBE NATURAL LUBRICANT - REGULAR, WARMING
Obstetrics & Gynecology
171d
Cleared
Mar 06, 2012
KIMONO MICROTHIN WITH AQUA LUBE, REALITY ULTRA LUBRICATED
Obstetrics & Gynecology
82d
Cleared
Dec 08, 2011
AQUA LUBE
Obstetrics & Gynecology
308d