FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

JWG-1

K Number: K252101 · Decision Mar 19, 2026
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
3
Review Days
259

Basic Information

Device Name
JWG-1
K Number
K252101
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Yamaha Motor Co., Ltd.
Date Received
July 3, 2025
Decision Date
March 19, 2026
Product Code
ITI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ITI Wheelchair, Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ITI), ordered by most recent decision date.

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Other Clearances by Yamaha Motor Co., Ltd.

K Number Device Name
K203806 JWX-1 Plus (Navigo 16/Navigo 24)
K140204 JWX-2