Cooper-Hewitt Electric Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cooper-Hewitt Electric Co. - FDA 510(k) Cleared Devices
8
Total
7
Cleared
0
Denied
Cooper-Hewitt Electric Co. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 1987. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cooper-Hewitt Electric Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cooper-Hewitt Electric Co.
8 devices
Cleared
Jan 13, 1987
AIR CARE AIR SANITIZER
General Hospital
364d
Cleared
Aug 06, 1986
SPERTILITE PHOTOTHERAPY LAMP
General & Plastic Surgery
29d
Cleared
Dec 02, 1981
AQUANOMICS, #SP36SF
General Hospital
35d
Cleared
Dec 02, 1981
AQUANOMICS, #HHU60
General Hospital
35d
Cleared
Dec 02, 1981
AQUANOMICS, MINI 60L
General Hospital
35d
Cleared
Dec 02, 1981
AQUANOMICS, #MP2SF
General Hospital
35d
Cleared
Dec 02, 1981
AQUANOMICS, #HHU100
General Hospital
35d
Cleared
Dec 02, 1981
AQUANOMICS, #MP4SF
General Hospital
35d