Last synced on 25 January 2026 at 3:41 am

ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202529
510(k) Type
Special
Applicant
Prosomnus Sleep Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
80 days
Submission Type
Summary

ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202529
510(k) Type
Special
Applicant
Prosomnus Sleep Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
80 days
Submission Type
Summary