Luminance Red Cold Sore Device (TN1927G)— 510(k) K251973
Substantially EquivalentLuminance Medical Ventures, Inc.
FDA 510(k) clearance K251973 for Luminance Red Cold Sore Device (TN1927G), Substantially Equivalent on 2025-09-23. Applicant: Luminance Medical Ventures, Inc.. Device class: 2.
Clearance details
- Applicant
- Luminance Medical Ventures, Inc.
- Product code
- Code OKJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4860
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
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