CS6101 Interferential Kit CS6101-2-K01 Interferential Kit
CS6101 Interferential Kit CS6101-2-K01 Interferential Kit is a Class II device made by Control Solutions, Inc., listed in FDA GUDID since 20 Mar 2023 (UDI-DI 00860009424722), 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 | Number00860009424722 | Date20 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 00860009424722
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CS6101 Interferential Kit
- Generic name
- Multi-modality physical therapy system, simultaneous, professional-use
- Model / reference
- CS6101-2-K01 Interferential Kit
- Primary DI / UDI-DI
- 00860009424722
- FDA product code
- LIH, QPL
- GMDN term
- Multi-modality physical therapy system, simultaneous, professional-use
- Device class
- Class II
- Regulation number
- 882.5890
- GUDID distribution status
- In Commercial Distribution
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