SKY Medical, a.s.

SKY Medical, a.s. — FDA 510(k) Submissions

SKY Medical, a.s. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gastrointestinal Tubes With Enteral Specific Connectors . Use the specialty filter in the sidebar to narrow results.