Prosomnous Sleep Technologies is one of 18378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prosomnous Sleep Technologies - FDA 510(k) Cleared Devices
Recent clearances: Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder
1
Total
1
Cleared
0
Denied
Prosomnous Sleep Technologies has 1 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Prosomnous Sleep Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prosomnous Sleep Technologies
1 devices