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HPO Exotic, LP1, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega Lux
FDA 510(k)Class II (US FDA 510(k))
510(k) K161394
Identifiers
- 510(k) Number
- K161394 FDA 510(k)
- FDA Product Code
- LEJ FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4635 FDA 510(k)
- Regulation Number
- 878.4635 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
HPO Exotic, LP1, LP2, LP3, Mastersun 360, Mastersun 360 New Reflector, Vega Lux by Sportarredo Group S.C. — Class II — FDA_510K — listed in FDA 510(k)
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 | K161394 | Class II | Active |
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Manufacturer
- Manufacturer
- Sportarredo Group S.C.
Sources (1)
- FDA 510(k) K161394 24 fields · synced Jun 18, 2026