Western Laboratories Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Western Laboratories Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Western Laboratories Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1978 to 1984. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Western Laboratories Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Western Laboratories Corp.
7 devices
Cleared
Jun 11, 1984
HEPARINOMETER
Chemistry
202d
Cleared
Apr 12, 1983
MODEL 200
Ophthalmic
56d
Cleared
Jul 02, 1982
MODEL 100 BICARBONATE CONDUCTIVITY
Gastroenterology & Urology
10d
Cleared
May 27, 1982
MODEL 80 BC
Gastroenterology & Urology
15d
Cleared
May 27, 1982
MODEL 90 BC
Gastroenterology & Urology
15d
Cleared
Jul 28, 1980
MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TEST
Gastroenterology & Urology
55d
Cleared
Aug 31, 1978
MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT
Gastroenterology & Urology
86d