WHILL Model M
by Whill, Inc.
510(k) K153543
WHILL Model M is a medical device (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Whill, Inc., cleared under FDA 510(k) K153543 on 12 Feb 2016, 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 | FDA 510(k)SESE | NumberK153543 | Date12 Feb 2016 | StatusActive |
Official records
- FDA 510(k) database K153543
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ITI
- Device class
- Class II
- Regulation
- 21 CFR Part 890.3860
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code ITI (Wheelchair, Powered).
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- TE-2000 POWER TILT/POWER ELEVATING SEAT COMBINATION SYSTEM by Accelerated Rehab Designs, Inc.