Merits P325 30200552
by Merits Health Products., Inc.
Merits P325 30200552 is a wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Merits Health Products., Inc., cleared under FDA 510(k) K012802 on 18 Sep 2001 and listed in FDA GUDID since 25 May 2018 (UDI-DI 04714379292053), 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 | Number04714379292053 | Date25 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK012802 | Date18 Sep 2001 | StatusActive |
Official records
- AccessGUDID record 04714379292053
- FDA 510(k) database K012802
Across registries
- FDA 510(k) K012802 decided 18 Sep 2001 Active
- FDA GUDID UDI-DI 04714379292053 listed 25 May 2018 Listed
Recalls
-
- Ongoing Z-1504-2021
Seat baseplate pin has broken in the field.
Timeline
- Cleared FDA 510(k) K012802
- Listed FDA GUDID 04714379292053
- 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- Withdrawn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
- P325 30200552
- Primary DI / UDI-DI
- 04714379292053
- 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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