Resmed Pty Ltd (Registration Number: 3004604967) is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Resmed Pty Ltd (Registration Number: 3004604967) - FDA 510(k) Cleared...
Recent clearances: AirFit F30i Mask System, Oran Park Mask, Whitsundays Mask System
3
Total
3
Cleared
0
Denied
Resmed Pty Ltd (Registration Number: 3004604967) has 3 FDA 510(k) cleared medical devices. Based in Bella Vista, AU.
Latest FDA clearance: Sep 2024. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Resmed Pty Ltd (Registration Number: 3004604967) Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Resmed Corp (Registration Number: 3007573469) and Remed Corp (Registration Number: 3007573469).
FDA 510(k) Regulatory Record - Resmed Pty Ltd (Registration Number: 3004604967)
3 devices