MOBILE VERSA LIGHT— 510(k) K111049
Substantially EquivalentMedtek Lighting Corp
FDA 510(k) clearance K111049 for MOBILE VERSA LIGHT, Substantially Equivalent on 2012-05-25. Applicant: Medtek Lighting Corp. Device class: 2.
Clearance details
- Applicant
- Medtek Lighting Corp
- Product code
- Code FTC
- Device class
- Class 2
- Regulation
- 21 CFR 878.4630
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Knoxville, TN, US
Recent devices under product code FTC
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