Visionbody— 510(k) K222386
Substantially EquivalentVb Technologies AG
FDA 510(k) clearance K222386 for Visionbody, Substantially Equivalent on 2023-02-24. Applicant: Vb Technologies AG. Device class: 2.
Clearance details
- Applicant
- Vb Technologies AG
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Zug, CH
Recent devices under product code NGX
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