Medical Device Manufacturer · US , Huntington , IN

Huntington Laboratories, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1985

Recent clearances: BEAUCOUP GENERAL PURPOSE DISINFECTANT, ASCEND GENERAL PURPOSE DISINFECTANT, MATAR GENERAL PURPOSE DISINFECTANT

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Huntington Laboratories, Inc. General Hospital ✕

7 devices

1-7 of 7

Cleared Mar 12, 1996

BEAUCOUP GENERAL PURPOSE DISINFECTANT

General Hospital · 29d

Cleared Mar 12, 1996

ASCEND GENERAL PURPOSE DISINFECTANT

General Hospital · 29d

Cleared Mar 12, 1996

MATAR GENERAL PURPOSE DISINFECTANT

General Hospital · 29d

Cleared Aug 11, 1995

FORMULATION HWS-128 EPA REG. NO. 47371-130

General Hospital · 44d

Cleared Aug 11, 1995

FORMULATION HWS-256 EPA REG. NO. 47371-129

General Hospital · 44d

Cleared Aug 11, 1995

FORMULATION HWS-64 EPA REG. NO. 47371-131

General Hospital · 44d

Cleared Nov 13, 1985

General Hospital · 71d

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 12, 2026