Vibrant System— 510(k) K232830
Substantially EquivalentVibrant, Ltd.
FDA 510(k) clearance K232830 for Vibrant System, Substantially Equivalent on 2023-12-08. Applicant: Vibrant, Ltd.. Device class: 2.
Clearance details
- Applicant
- Vibrant, Ltd.
- Product code
- Code QTN
- Device class
- Class 2
- Regulation
- 21 CFR 876.5940
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Yokneam, IL
Recent devices under product code QTN
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