Merits P322-Barmub
by Merits Health Products., Inc.
Merits P322-Barmub is a wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Merits Health Products., Inc., cleared under FDA 510(k) K122357 on 9 Jan 2013 and listed in FDA GUDID since 4 May 2017 (UDI-DI 04714379291926), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04714379291926 | Date4 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122357 | Date9 Jan 2013 | StatusActive |
Official records
- AccessGUDID record 04714379291926
- FDA 510(k) database K122357
Across registries
- FDA 510(k) K122357 decided 9 Jan 2013 Active
- FDA GUDID UDI-DI 04714379291926 listed 4 May 2017 Listed
Recalls
-
- Ongoing Z-1504-2021
Seat baseplate pin has broken in the field.
Timeline
- Cleared FDA 510(k) K122357
- Listed FDA GUDID 04714379291926
- Recall initiated FDA recalls Z-1504-2021
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Merits
- Generic name
- Wheelchair, power-assisted, occupant-controlled, non-collapsible
- Model / reference
- P322-BARMUB
- Primary DI / UDI-DI
- 04714379291926
- 510(k) Number
- FDA product code
- ITI
- GMDN term
- Wheelchair, power-assisted, occupant-controlled, non-collapsible
- Device class
- Class II
- Regulation number
- 890.3860
- GUDID distribution status
- In Commercial Distribution
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