Dilab, Inc.

Dilab, Inc. — FDA 510(k) Submissions

Dilab, Inc. has submitted 11 FDA 510(k) premarket notifications since 1985, of which 11 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Biuret (colorimetric), Total Protein, Diacetyl-monoxime, Urea Nitrogen, Lieberman-burchard/abell-kendall, Colorimetric, Cholesterol, Antistreptolysin - Titer/streptolysin O Reagent, Cresolphthalein Complexone, Calcium . Use the specialty filter in the sidebar to narrow results.