Allied Instrumentation Laboratory is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allied Instrumentation Laboratory - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Allied Instrumentation Laboratory has 7 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 7 cleared submissions from 1985 to 1986. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Allied Instrumentation Laboratory Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allied Instrumentation Laboratory
7 devices
Cleared
Jun 17, 1986
MULTI-4 CO-OXIMETER CONTROL
Chemistry
32d
Cleared
Mar 17, 1986
PHENOBARBITAL TEST SYSTEM
Toxicology
42d
Cleared
Mar 05, 1986
IL TEST PHENYTOIN
Toxicology
36d
Cleared
Oct 15, 1985
IL TEST THEOPHYLLINE ASSAY
Toxicology
29d
Cleared
Jul 22, 1985
IL SYSTEM 1304 & 1306, PH/BLOOD GAS ANALYZERS
Chemistry
28d
Cleared
Jun 10, 1985
CLINICAL CHEMISTRY ANALYTICAL SYSTEM
Chemistry
39d
Cleared
Apr 03, 1985
I-L TEST, DIRECT BILIRUBIN SET
Chemistry
37d