Ansell, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ansell, Inc. Obstetrics & Gynecology ✕
12 devices
Cleared
Jul 21, 1999
ANSELL CONDOMS
Obstetrics & Gynecology
225d
Cleared
Jul 06, 1999
LIFESTYLES XTRA PLEASURE
Obstetrics & Gynecology
272d
Cleared
Dec 19, 1995
SPERMICIDALLY LUBRICATED CONDOM
Obstetrics & Gynecology
713d
Cleared
Jan 30, 1995
CONDOM
Obstetrics & Gynecology
390d
Cleared
Jan 30, 1995
NON-LUBRICATED CONDOM
Obstetrics & Gynecology
390d
Cleared
Mar 27, 1990
NUDA (CURRENTLY CALLED ULTRA SENSITIVE)
Obstetrics & Gynecology
18d
Cleared
Mar 27, 1990
G.S.A. COLORED CONDOMS
Obstetrics & Gynecology
18d
Cleared
Oct 20, 1988
KISS OF MINT(TM) NON-LUBRICATED CONDOM
Obstetrics & Gynecology
132d
Cleared
Jun 11, 1987
LIFESTYLES EXTRA STRENGTH CONDOMS W/NONOXYNOL-9
Obstetrics & Gynecology
71d
Cleared
Feb 02, 1987
EXTRA STRONG CONDOM
Obstetrics & Gynecology
88d
Cleared
Mar 31, 1983
PRIME
Obstetrics & Gynecology
30d
Cleared
Sep 30, 1982
NUDA-PLUS CONDOM W/SPERMICIDAL LUBRICANT
Obstetrics & Gynecology
15d