510(k) K222201
K222201 is an FDA 510(k) premarket notification submitted by Medlander Medical Technology, Inc. for the device "Biological Feedback and Stimulation System". The FDA issued a decision of Substantially Equivalent on Oct 21, 2022. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 21, 2022
- Date Received
- Jul 25, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type
- 510(k)