RT300 Clinic Replacement (SA to SA)
by Restorative Therapies, Inc.
RT300 Clinic Replacement (SA to SA) is a Class II device made by Restorative Therapies, Inc., listed in FDA GUDID since 10 Aug 2017 (UDI-DI SA219216), registry data as of 23 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 | NumberSA219216 | Date10 Aug 2017 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- RT300
- Generic name
- Physical therapy transcutaneous electrical stimulation system, line-powered
- Model / reference
- RT300 Clinic Replacement (SA to SA)
- Primary DI / UDI-DI
- SA219216
- FDA product code
- GZI
- GMDN term
- Physical therapy transcutaneous electrical stimulation system, line-powered
- Device class
- Class II
- Regulation number
- 882.5810
- GUDID distribution status
- In Commercial Distribution
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