Altaviz, LLC

Altaviz, LLC — FDA 510(k) Submissions

Altaviz, LLC has submitted 3 FDA 510(k) premarket notifications since 2022, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Ophthalmic Syringe . Use the specialty filter in the sidebar to narrow results.