Medical Device Manufacturer · US , Mchenry , IL

Secol Co. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1980

Recent clearances: SOLVALINE, CELLONA PLASTER VARNISH, METAL SPLINTS

18

Total

18

Cleared

0

Denied

Secol Co. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1980 to 1981.

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

Secol Co. is one of 5820 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Secol Co.

18 devices

1-12 of 18

Cleared Feb 13, 1981

General Hospital · 101d

Cleared Feb 04, 1981

CELLONA PLASTER VARNISH

Physical Medicine · 19d

Cleared Jan 26, 1981

Physical Medicine · 10d

Cleared Jan 26, 1981

COBBLER'S CHIP SPLINTS

Orthopedic · 10d

Cleared Dec 22, 1980

PRO-OPHTA STICKS

Ophthalmic · 48d

Cleared Dec 18, 1980

LOMATUELL OINTMENT DRESSING

General & Plastic Surgery · 44d

Cleared Dec 17, 1980

POROPLAST-EYE DRESSING

Ophthalmic · 43d

Cleared Dec 17, 1980

METALLINE DRESSINGS

General Hospital · 43d

Cleared Dec 17, 1980

ZINC PASTE BANDAGE

General & Plastic Surgery · 43d

Cleared Dec 17, 1980

General Hospital · 43d

Cleared Dec 17, 1980

General & Plastic Surgery · 43d

Cleared Dec 11, 1980

ELASTIC BANDAGE

General Hospital · 37d