Western Advanced Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Western Advanced Technology, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Western Advanced Technology, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1980 to 1983. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Western Advanced Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Western Advanced Technology, Inc.
6 devices
Cleared
Jul 12, 1983
SYSTEM 80 FACEPLATE-IN-THE-EAR #F1
Dental
336d
Cleared
Jan 19, 1982
AUDITORY STIMULATOR
Ear, Nose, Throat
28d
Cleared
Aug 20, 1981
TENS DEVICE
Neurology
23d
Cleared
Jul 15, 1981
AUDITORY LOCALIZER
Ear, Nose, Throat
23d
Cleared
Jul 15, 1981
OCTOTOXIC SCREENER
Ear, Nose, Throat
21d
Cleared
Oct 10, 1980
E1 SERIES HEARING AID
Ear, Nose, Throat
17d