Tampax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tampax, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Tampax, Inc. has 12 FDA 510(k) cleared obstetrics & gynecology devices. Based in Walker, US.
Historical record: 12 cleared submissions from 1978 to 1983.
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 - Tampax, Inc.
12 devices
Cleared
Nov 28, 1983
DEODORANT MAXITHINS PANTY SHIELD
Obstetrics & Gynecology
88d
Cleared
Nov 28, 1983
REGULAR DEODORANT MAXITHINS PADS
Obstetrics & Gynecology
88d
Cleared
Nov 28, 1983
TAMPAX SUPER DEODORANT MAXITHINS
Obstetrics & Gynecology
88d
Cleared
Oct 14, 1983
MAXITHINS UNSCENTED PANTY SHIELDS
Obstetrics & Gynecology
43d
Cleared
Jun 25, 1982
REGULAR MAXITHINS PADS & SUPER MAXITHINS
Obstetrics & Gynecology
18d
Cleared
Mar 18, 1982
TAMPAX TAMPONS
Obstetrics & Gynecology
56d
Cleared
Jan 25, 1982
PETAL SOFT PLASTIC APPLICATOR TAMPAX
Obstetrics & Gynecology
26d
Cleared
Mar 04, 1981
TAMPAX DEODORANT TAMPONS
Obstetrics & Gynecology
42d
Cleared
Jan 28, 1981
TAMPAX MAXITHINS PADS
Obstetrics & Gynecology
6d
Cleared
Jan 12, 1981
PETAL SOFT PLASTIC APPLICATOR TAMPAX
Obstetrics & Gynecology
68d
Cleared
May 14, 1980
TAMPAX TAMPONS
Obstetrics & Gynecology
36d
Cleared
May 31, 1978
MODIFIED UNTREATED TAMPAX TAMPONS
Obstetrics & Gynecology
44d