510(k) K201258
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 1, 2021
- Date Received
- May 11, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, Blood Glucose, Over The Counter
- Device Class
- Class II
- Regulation Number
- 862.1345
- Review Panel
- CH
- Submission Type