510(k) K222010
K222010 is an FDA 510(k) premarket notification submitted by Biobeat Technologies , Ltd. for the device "Biobeat Platform-2 and BB-613WP Patch". The FDA issued a decision of Substantially Equivalent on December 30, 2022. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Biobeat Technologies , Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 30, 2022
- Date Received
- July 7, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oximeter
- Device Class
- Class II
- Regulation Number
- 870.2700
- Review Panel
- AN
- Submission Type