# K240119: VasQ

- Pathway: 510(k) (Special)
- Applicant: Laminate Medical Technologies, Ltd.
- Decided: Feb 16, 2024 after 31 days
- Product code: QVQ (Extravascular Support For An Arteriovenous Fistula For Vascular Access)
- Device class: 2
- Regulation: 21 CFR 870.4600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to DEN220026 (2023). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- DEN220026: VasQ, Laminate Medical Technologies, Ltd. (2023) Summary page 5.

## Indications for use
VasQ is intended for use as an external support for upper extremity arteriovenous fistulas created for vascular access by means of vascular surgery.

Source page: https://510kreport.com/device/K240119
Methodology: https://510kreport.com/methodology