WC Bari 22 WC22
WC Bari 22 WC22 is a bariatric wheelchair (FDA Class I; FDA product code IOR, Wheelchair, Mechanical) made by Sizewise Rentals, L.L.C., cleared under FDA 510(k) K883034 on 2 Aug 1988 and listed in FDA GUDID since 7 Feb 2019 (UDI-DI 00845699000104), 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 | Number00845699000104 | Date7 Feb 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK883034 | Date2 Aug 1988 | StatusActive |
Official records
- AccessGUDID record 00845699000104
- FDA 510(k) database K883034
Across registries
- FDA 510(k) K883034 decided 2 Aug 1988 Active
- FDA GUDID UDI-DI 00845699000104 listed 7 Feb 2019 Listed
Timeline
- Cleared FDA 510(k) K883034
- Listed FDA GUDID 00845699000104
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- WC Bari 22
- Generic name
- Bariatric wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible
- Model / reference
- WC22
- Primary DI / UDI-DI
- 00845699000104
- 510(k) Number
- FDA product code
- IOR
- GMDN term
- Bariatric wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible
- Device class
- Class I
- Regulation number
- 890.3850
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code IOR (Wheelchair, Mechanical).
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- CAPELLA by Future Mobility Healthcare, Inc.
- KENSTONE by Kenda USA
- BRIX WHEELCHAIR by Meyra, Inc.
- HUAYI K-SERIES LIGHTWEIGHT WHEELCHAIR K3/K4 by Danyang Huayi Medical Supply & Equipment Co, Ltd.