FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)

K Number: K232193 · Decision Sep 22, 2023
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
3
Review Days
59

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Basic Information

Device Name
Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)
K Number
K232193
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Yurob Rehabilitation Medical Co., Ltd.
Date Received
July 25, 2023
Decision Date
September 22, 2023
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 Yurob Rehabilitation Medical Co., Ltd.

K Number Device Name
K253600 Scooter (YD-03)
K253980 Electrically Powered Wheelchair (Model YC-01)