Toxi-Lab, Inc.

Toxi-Lab, Inc. — FDA 510(k) Submissions

Toxi-Lab, Inc. has submitted 5 FDA 510(k) premarket notifications since 1990, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drug Mixture Control Materials, Reagents, Test, Tetrahydrocannabinol, Potassium Dichromate, Alcohol, Nad-nadh, Specific Reagent For Alcohol Enzyme Method, Thin Layer Chromatography, Opiates . Use the specialty filter in the sidebar to narrow results.