510(k) K221823
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 2022
- Date Received
- June 23, 2022
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Neuromuscular, External Functional
- Device Class
- Class II
- Regulation Number
- 882.5810
- Review Panel
- NE
- Submission Type