← Back to catalogue
CureLight Medical Diode Laser Systems - CureLight F2-B15
FDA 510(k)Class II (US FDA 510(k))
510(k) K253965
Identifiers
- 510(k) Number
- K253965 FDA 510(k)
- FDA Product Code
- ILY FDA 510(k)
- Models / Variants
- CureLight F2-B15 FDA 510(k)CureLight F2-A30 FDA 510(k)CureLight F2-B30 FDA 510(k)CureLight F3-AB30 FDA 510(k)CureLight F3-AB60.) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 890.5500 FDA 510(k)
- Regulation Number
- 890.5500 FDA 510(k)
- Advisory Committee
- Physical Medicine FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
CureLight Medical Diode Laser Systems - CureLight F2-B15 by Wuhan PHOMED Technology Company , 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 | K253965 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Wuhan PHOMED Technology Company , Ltd.
Sources (1)
- FDA 510(k) K253965 24 fields · synced Jun 19, 2026