LAFACI— 510(k) K032400
Substantially EquivalentVision Pro, LLC
FDA 510(k) clearance K032400 for LAFACI, Substantially Equivalent on 2004-05-07. Applicant: Vision Pro, LLC. Device class: 2.
Clearance details
- Applicant
- Vision Pro, LLC
- Product code
- Code FYD
- Device class
- Class 2
- Regulation
- 21 CFR 878.5070
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.