Merits S13151ARMU
by Merits Health Products., Inc.
Merits S13151ARMU is an assistive scooter (FDA Class II; FDA product code INI, Vehicle, Motorized 3-Wheeled) made by Merits Health Products., Inc., cleared under FDA 510(k) K011751 on 6 Aug 2001 and listed in FDA GUDID since 12 Sep 2016 (UDI-DI 04714379291711), 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 | Number04714379291711 | Date12 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK011751 | Date6 Aug 2001 | StatusActive |
Official records
- AccessGUDID record 04714379291711
- FDA 510(k) database K011751
Across registries
- FDA 510(k) K011751 decided 6 Aug 2001 Active
- FDA GUDID UDI-DI 04714379291711 listed 12 Sep 2016 Listed
Recalls
-
- Ongoing Z-1505-2021
Seat baseplate pin has broken in the field.
Timeline
- Cleared FDA 510(k) K011751
- Listed FDA GUDID 04714379291711
- Recall initiated FDA recalls Z-1505-2021
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Merits
- Generic name
- Assistive scooter, electric-motor-driven
- Model / reference
- S13151ARMU
- Primary DI / UDI-DI
- 04714379291711
- 510(k) Number
- FDA product code
- INI
- GMDN term
- Assistive scooter, electric-motor-driven
- Device class
- Class II
- Regulation number
- 890.3800
- GUDID distribution status
- In Commercial Distribution
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