Pegasus DC02
by Anhui JBH Medical Apparatus Co., Ltd.
Pegasus DC02 is an electric-motor-driven wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Anhui JBH Medical Apparatus Co., Ltd., cleared under FDA 510(k) K242252 on 27 Dec 2024 and listed in FDA GUDID since 4 Sep 2025 (UDI-DI 06973175531003), active as of 22 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 | Number06973175531003 | Date4 Sep 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK242252 | Date27 Dec 2024 | StatusActive |
Official records
- AccessGUDID record 06973175531003
- FDA 510(k) database K242252
Across registries
- FDA 510(k) K242252 decided 27 Dec 2024 Active
- FDA GUDID UDI-DI 06973175531003 listed 4 Sep 2025 Listed
Timeline
- Cleared FDA 510(k) K242252
- Listed FDA GUDID 06973175531003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Pegasus
- Generic name
- Electric-motor-driven wheelchair, occupant-controlled
- Model / reference
- DC02
- Primary DI / UDI-DI
- 06973175531003
- 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.