Arrow International, LLC

Arrow International, LLC — FDA 510(k) Submissions

Arrow International, LLC has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Balloon, Intra-aortic And Control, Anesthesia Conduction Kit . Use the specialty filter in the sidebar to narrow results.