Warrior WL600
by Harmar Summit, LLC 12 variants
Warrior (WL600DC) is a stairlift (FDA Class II; FDA product code ILK, Transport, patient, powered) made by Harmar Summit, LLC, cleared under FDA 510(k) K091858 on 1 Jul 2009 and listed in FDA GUDID since 28 Sep 2016 (UDI-DI 00817650022487), 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 | Number00817650022487 | Date28 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK091858 | Date1 Jul 2009 | StatusActive |
Official records
- AccessGUDID record 00817650022487
- FDA 510(k) database K091858
Across registries
- FDA 510(k) K091858 decided 1 Jul 2009 Active
- FDA GUDID UDI-DI 00817650022487 listed 28 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K091858
- Listed FDA GUDID 00817650022487
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Warrior
- Generic name
- Stairlift, chair
- Model / Ref / Catalog
- WL600, WL600DC
- Primary DI / UDI-DI
- 00817650022487
- 510(k) Number
- FDA product code
- ILK
- GMDN term
- Stairlift, chair
- Device class
- Class II
- Regulation number
- 890.5150
- GUDID distribution status
- In Commercial Distribution
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