Vibrant System— 510(k) DEN210052
UnknownVibrant, Ltd.
FDA 510(k) clearance DEN210052 for Vibrant System, Unknown on 2022-08-26. 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
- Unknown
- Clearance type
- Direct
- Location
- Yokneam, IL
Recent devices under product code QTN
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