Burt M1200
Burt M1200 is a virtual-display rehabilitation system (FDA Class II; FDA product code IKK, System, Isokinetic Testing And Evaluation) made by Barrett Technology, LLC, listed in FDA GUDID since 14 Nov 2017 (UDI-DI 00867504000406), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00867504000406 | Date14 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 00867504000406
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Burt
- Generic name
- Virtual-display rehabilitation system, powered-support, upper-limb
- Model / reference
- M1200
- Primary DI / UDI-DI
- 00867504000406
- FDA product code
- IKK
- GMDN term
- Virtual-display rehabilitation system, powered-support, upper-limb
- Device class
- Class II
- Regulation number
- 890.1925
- GUDID distribution status
- In Commercial Distribution
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