WHILL Model F— 510(k) K221438

Name: FDA 510(k) clearance K221438
Creator: U.S. Food and Drug Administration
Published: 2022-06-07

Substantially Equivalent

Whill, Inc.

FDA 510(k) clearance K221438 for WHILL Model F, Substantially Equivalent on 2022-06-07. Applicant: Whill, Inc.. Device class: 2.

Clearance details

Applicant: Whill, Inc.
Product code: Code ITI
Device class: Class 2
Regulation: 21 CFR 890.3860
Advisory panel: Physical Medicine
Date received: 2022-05-17
Decision date: 2022-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shinagawa-Ku, JP

Download summary PDF View on FDA.gov ↗

Recent devices under product code ITI

view all

K260053 — Power Wheelchair (OS-R-M01I)2026-09-08
K260229 — Electric wheelchair (HC819N, HC830N, HC831N)2026-09-08
K261354 — Electric wheelchair (D03)2026-08-21
K261149 — Electric Wheelchair (DY611A-2, DY612A-1)2026-07-10
K261396 — Electric Wheelchair2026-07-08

More clearances from Whill, Inc.

view all

K261175 — WHILL (WHILL Model C2)2026-06-12
K242760 — WHILL Model R2025-01-06
K213383 — WHILL Model C22021-11-09
K153543 — WHILL Model M2016-02-12

Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.