Mayer Laboratories - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Mayer Laboratories has 16 FDA 510(k) cleared obstetrics & gynecology devices. Based in Oakland, US.
Historical record: 16 cleared submissions from 1987 to 2001.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Oct 24, 2001
EZ-ON CONDOM
Obstetrics & Gynecology
482d
Cleared
Nov 08, 1995
KIMONO MICROTHIN
Obstetrics & Gynecology
329d
Cleared
Sep 22, 1995
KIMONO (CONDOMS)
Obstetrics & Gynecology
476d
Cleared
Sep 22, 1995
MAXX
Obstetrics & Gynecology
282d
Cleared
Jan 06, 1994
SHEATHES, STERILE SHEATHES
Radiology
413d
Cleared
Jul 22, 1993
DIGITEX, DIGITEX HYPOALLERGENIC
General Hospital
233d
Cleared
Nov 26, 1990
KIMONO PLUS
Obstetrics & Gynecology
62d
Cleared
Nov 23, 1990
LABELLING MODIFICATION TO MAXX PLUS
Obstetrics & Gynecology
57d
Cleared
Nov 20, 1990
ORION PLUS/MODIFICATION
Obstetrics & Gynecology
27d
Cleared
Nov 28, 1989
STANDARD CONDOM
Obstetrics & Gynecology
76d
Cleared
Mar 31, 1989
SUPER MAXX OTHERS (MULTIPLE) CONDOMS
Obstetrics & Gynecology
157d
Cleared
Mar 31, 1989
ORION PLUS W/NONOXYNOL-9 OTHERS (MULTIPLE) CONDOMS
Obstetrics & Gynecology
157d
Cleared
Mar 31, 1989
KIMONO PLUS OTHERS (MULTIPLE) CONDOMS
Obstetrics & Gynecology
157d
Cleared
Apr 06, 1988
CONDOMS (HOMBRE BLACK/BLACK SATIN/XT-12/ORION)
Obstetrics & Gynecology
293d
Cleared
Jan 21, 1988
XL-4 PAGODA (CONDOMS)
Obstetrics & Gynecology
57d
Cleared
Dec 08, 1987
KIMONO (CONDOMS)
Obstetrics & Gynecology
146d