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IPL Hair Removal Device (MLY-M011) +5 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K251914
Identifiers
- 510(k) Number
- K251914 FDA 510(k)
- FDA Product Code
- OHT FDA 510(k)
- Models / Variants
- IPL Hair Removal Device (MLY-M011) FDA 510(k)IPL Hair Removal Device (MLY-M012) FDA 510(k)IPL Hair Removal Device (MLY-M013) FDA 510(k)IPL Hair Removal Device (MLY-M015) FDA 510(k)IPL Hair Removal Device (MLY-T001) FDA 510(k)IPL Hair Removal Device (MLY-T002) 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)
IPL Hair Removal Device (MLY-M011) +5 more models by Miley Technology (Hebei) Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 6 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 | K251914 | Class II | Active |
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Manufacturer
- Manufacturer
- Miley Technology (Hebei) Co., Ltd.
Sources (1)
- FDA 510(k) K251914 24 fields · synced Jun 18, 2026