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Electrically Power Wheelchairs (Models:YLB-W-0812-A01 +2 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K232193
Identifiers
- 510(k) Number
- K232193 FDA 510(k)
- FDA Product Code
- ITI FDA 510(k)
- Models / Variants
- Models:YLB-W-0812-A01 FDA 510(k)YLB-W-0812-A02 FDA 510(k)YLB-W-0812-A03 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 890.3860 FDA 510(k)
- Regulation Number
- 890.3860 FDA 510(k)
- Advisory Committee
- Physical Medicine FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Electrically Power Wheelchairs (Models:YLB-W-0812-A01 +2 more) by Yurob Rehabilitation Medical Co., Ltd — Class II — FDA_510K — listed in FDA 510(k) — 3 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K232193 | Class II | Active |
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Manufacturer
- Manufacturer
- Yurob Rehabilitation Medical Co., Ltd
- FDA Applicant
- Yurob Rehabilitation Medical Co., Ltd.
Sources (1)
- FDA 510(k) K232193 24 fields · synced Jun 18, 2026