510(k) K213971
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 3, 2022
- Date Received
- December 20, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Photoplethysmograph Analysis Software For Over-The-Counter Use
- Device Class
- Class II
- Regulation Number
- 870.2790
- Review Panel
- CV
- Submission Type
A photoplethysmograph analysis software device for over-the-counter use analyzes photoplethysmograph data and provides information for identifying irregular heart rhythms. This device is not intended to provide a diagnosis.