Anatech, Ltd.

Anatech, Ltd. — FDA 510(k) Submissions

Anatech, Ltd. has submitted 14 FDA 510(k) premarket notifications since 1984, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Formalin, Neutral Buffered, Hematoxylin, Agent, Clearing, Hematoxylin Harris's, Formaldehyde (formalin, Formol) . Use the specialty filter in the sidebar to narrow results.