Lifevac, LLC

Lifevac, LLC — FDA 510(k) Submissions

Lifevac, LLC has submitted 1 FDA 510(k) premarket notifications since 2026, of which 0 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suction Anti-choking Device As A Second-line Treatment . Use the specialty filter in the sidebar to narrow results.