Huntington Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Huntington Laboratories, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Huntington Laboratories, Inc. has 7 FDA 510(k) cleared medical devices. Based in Huntington, US.
Historical record: 7 cleared submissions from 1985 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Huntington Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Huntington Laboratories, Inc.
7 devices
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
SANA-LUBE
General Hospital
71d