Resmed Sas is one of 18437 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Resmed Sas - FDA 510(k) Cleared Devices
Recent clearances: Narval Brux, NARVAL CC
2
Total
2
Cleared
0
Denied
Resmed Sas has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Resmed Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Resmed Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Resmed Sas
2 devices