Surgipath

Surgipath — FDA 510(k) Submissions

Surgipath has submitted 12 FDA 510(k) premarket notifications since 1981, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stain, Papanicolau, Hematoxylin, Media, Mounting, Oil Soluble, Hematoxylin Harris's, Solution, Decalcifier, Acid Containing . Use the specialty filter in the sidebar to narrow results.