Intl. Playtex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Playtex, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Intl. Playtex, Inc. has 10 FDA 510(k) cleared obstetrics & gynecology devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1987.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Playtex, Inc.
10 devices
Cleared
May 12, 1987
PLAYTEX TAMPONS AND DEODORANT TAMPONS
Obstetrics & Gynecology
49d
Cleared
Jul 22, 1986
PLAYTEX TAMPONS
Obstetrics & Gynecology
77d
Cleared
Nov 21, 1985
PLAYTEX LIGHT'N GENTLE UNSCENTED/DEODORANT/MINI TA
Obstetrics & Gynecology
30d
Cleared
May 22, 1985
PLAYTEX SLENDER REG. TAMPONS & DEODORANT TAMPONS
Obstetrics & Gynecology
9d
Cleared
Apr 12, 1985
PLAYTEX SUPER PLUS TAMPONS & DEODORANT TAMPONS
Obstetrics & Gynecology
8d
Cleared
Apr 12, 1985
PLAYTEX SUPER TAMPONS & SUPER DEODORANT TAMPONS
Obstetrics & Gynecology
8d
Cleared
Jan 08, 1979
PADS, MINI, MAXI DEODORANT
Obstetrics & Gynecology
21d
Cleared
Jan 08, 1979
PADS, MINI, MAXI
Obstetrics & Gynecology
21d
Cleared
Sep 13, 1976
TAMPON, PLAYTEX 2 VERSION A
Obstetrics & Gynecology
32d
Cleared
Aug 26, 1976
TAMPON, PLAYTEX 2 VERSION B
Obstetrics & Gynecology
14d