Life Technologies, Inc.

Life Technologies, Inc. — FDA 510(k) Submissions

Life Technologies, Inc. has submitted 4 FDA 510(k) premarket notifications since 1995, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula, Intrauterine Insemination, Media, Culture, Ex Vivo, Tissue And Cell . Use the specialty filter in the sidebar to narrow results.