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Ice Cooling IPL Hair Removal Device - UI07 GP
FDA 510(k)Class II (US FDA 510(k))
510(k) K240649
Identifiers
- 510(k) Number
- K240649 FDA 510(k)
- FDA Product Code
- OHT FDA 510(k)
- Models / Variants
- UI07 BR FDA 510(k)UI07 DB FDA 510(k)UI07 BL FDA 510(k)UI07 GP FDA 510(k)UI07 PN FDA 510(k)UI07 RE FDA 510(k)UI07 WH FDA 510(k)UI07 PW FDA 510(k)UI20 BR FDA 510(k)UI20 DB FDA 510(k)UI20 BL FDA 510(k)UI20GP FDA 510(k)UI20 PN FDA 510(k)UI20 RE FDA 510(k)UI20 WH FDA 510(k)UI20 PW 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)
Ice Cooling IPL Hair Removal Device - UI07 GP by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 16 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 | K240649 | Class II | Active |
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Manufacturer
- Manufacturer
- Shenzhen Ulike Smart Electronics Co., Ltd.
Sources (1)
- FDA 510(k) K240649 24 fields · synced Jun 18, 2026