← Back to catalogue
Ice Cooling IPL Hair Removal Device - UI06 RD
FDA 510(k)Class II (US FDA 510(k))
510(k) K240652
Identifiers
- 510(k) Number
- K240652 FDA 510(k)
- FDA Product Code
- OHT FDA 510(k)
- Models / Variants
- UI06 PN FDA 510(k)UI06 PL FDA 510(k)UI06 JL FDA 510(k)UI06 BR FDA 510(k)UI06 DB FDA 510(k)UI06 PR FDA 510(k)UI06 OG FDA 510(k)UI06 RD FDA 510(k)UI06 WH FDA 510(k)UI06 MG FDA 510(k)UI06 OB FDA 510(k)UI06 LY FDA 510(k)UI06 IG FDA 510(k)UIM20 GR FDA 510(k)UIM20 BK FDA 510(k)UIM20 SL FDA 510(k)UIM20 CB FDA 510(k)UIM20 WR 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 - UI06 RD by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 18 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 | K240652 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shenzhen Ulike Smart Electronics Co., Ltd.
Sources (1)
- FDA 510(k) K240652 24 fields · synced Jun 18, 2026