DEN220026
- 510(k) number
- DEN220026
- Device name
- VasQ
- Applicant
- Laminate Medical Technologies , Ltd. IL
- Product code
- QVQ — Extravascular Support For An Arteriovenous Fistula F
- Decision date
- 2023-09-26
- Date received
- 2022-04-29
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- Cardiovascular
Official FDA record: DEN220026
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.