Battery Powered Wheelchair GP130
Battery Powered Wheelchair GP130 is an electric-motor-driven wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Golden Brothers, Inc, cleared under FDA 510(k) K011153 on 29 May 2001 and listed in FDA GUDID since 12 Aug 2025 (UDI-DI B247GP130), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB247GP130 | Date12 Aug 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK011153 | Date29 May 2001 | StatusActive |
Official records
- FDA 510(k) database K011153
Across registries
- FDA 510(k) K011153 decided 29 May 2001 Active
- FDA GUDID UDI-DI B247GP130 listed 12 Aug 2025 Listed
Timeline
- Cleared FDA 510(k) K011153
- Listed FDA GUDID B247GP130
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Battery Powered Wheelchair
- Generic name
- Electric-motor-driven wheelchair, occupant-controlled
- Model / reference
- GP130
- Primary DI / UDI-DI
- B247GP130
- 510(k) Number
- FDA product code
- ITI
- GMDN term
- Electric-motor-driven wheelchair, occupant-controlled
- Device class
- Class II
- Regulation number
- 890.3860
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Electric-motor-driven wheelchair, occupant-controlled.