Medical Device Manufacturer · JP , Chuo-Ku, Gokyo 103 Japan

Kao Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1984

Total

Cleared

Denied

Kao Corp. has 9 FDA 510(k) cleared medical devices. Based in Chuo-Ku, Gokyo 103 Japan, JP.

Historical record: 9 cleared submissions from 1984 to 1989. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Kao Corp. Filter by specialty or product code using the sidebar.

Kao Corp. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kao Corp.

9 devices

1-9 of 9

Cleared Aug 11, 1989

LAURIER SANITARY NAPKIN

K893773 · HHD

Obstetrics & Gynecology · 81d

Cleared Aug 05, 1988

LAURIER SANITARY NAPKIN

K882768 · HHD

Obstetrics & Gynecology · 30d

Cleared Aug 05, 1987

LAURIER NIGHT SAFE EXTRA PROTECTION SANITARY NAP.

K872481 · HHD

Obstetrics & Gynecology · 43d

Cleared Jul 30, 1986

LAURIER SANTARY NAPKIN (MODIFICATION)

K862269 · HHD

Obstetrics & Gynecology · 47d

Cleared Jul 07, 1986

LAURIER OVERNIGHT SANITARY NAPKIN (MODIFICATION)

K862270 · HHD

Obstetrics & Gynecology · 24d

Cleared Jul 07, 1986

LAURIER SAFETY LONG SANITARY NAPKIN (MODIFICATION)

K862271 · HHD

Obstetrics & Gynecology · 24d

Cleared Aug 27, 1985

LAURIER SAFETY LONG SANITORY NAPKIN

K852924 · HHD

Obstetrics & Gynecology · 49d

Cleared Aug 26, 1985

LAURIER OVERNIGHT SANITARY NAPKIN

K852922 · HHD

Obstetrics & Gynecology · 48d

Cleared Oct 15, 1984

LAURIER SANITARY NAPKIN

K843318 · HHD

Obstetrics & Gynecology · 52d

Kao Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kao Corp.

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