Medical Device Manufacturer · AU , Bella Vista

Resmed Pty Ltd (Registration Number: 3004604967) - FDA 510(k) Cleared...

3 submissions · 3 cleared · Since 2023

Total

Cleared

Denied

FDA 510(k) Regulatory Record - Resmed Pty Ltd (Registration Number: 3004604967) Anesthesiology ✕

3 devices

1-3 of 3

Regulatory consultants 510(k) submission support ecosystem

Resmed Corp (Registration Number: 3007573469)

Remed Corp (Registration Number: 3007573469)

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 11, 2026