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Facial & Body Beauty Device - F3222 Pro
FDA 510(k)Class II (US FDA 510(k))
510(k) K253833
Identifiers
- 510(k) Number
- K253833 FDA 510(k)
- FDA Product Code
- OHS FDA 510(k)
- Models / Variants
- model: INIA-BD001 FDA 510(k)INIA-BD002 FDA 510(k)INIA-BD003 FDA 510(k)INIA-BD004 FDA 510(k)F2C15 FDA 510(k)F3222 Pro FDA 510(k)F5516 FDA 510(k)F3606 FDA 510(k)F2210 Pro FDA 510(k)F5808 FDA 510(k)INIA-ED001 FDA 510(k)INIA-ED002 FDA 510(k)INIA-BLD001 FDA 510(k)E1507 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4810 FDA 510(k)
- Regulation Number
- 878.4810 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Facial & Body Beauty Device - F3222 Pro by Shenzhen Jianchao Intelligent Technology Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 14 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 | K253833 | Class II | Active |
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Manufacturer
- Manufacturer
- Shenzhen Jianchao Intelligent Technology Co., Ltd.
Sources (1)
- FDA 510(k) K253833 24 fields · synced Jun 18, 2026