# K101838: VTS1000

- Pathway: 510(k) (Traditional)
- Applicant: Vuetek Scientific, LLC
- Decided: Feb 18, 2011 after 232 days
- Product code: KZA (Device, Vein Location, Liquid Crystal)
- Device class: 1
- Regulation: 21 CFR 880.6970
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Vustik® (Vustik, Inc.): named in the summary without a submission number
- (no number) Head Mounted Display (Vista Medical): named in the summary without a submission number

## Most influential descendants
- K152088: IV-eye (2016), 0 descendants of its own

## Indications for use
The VTS1000 is a non-invasive electronic device to aid in the visualization of superficial vasculature. It is indicated for use in procedures requiring vascular or peripheral vessel access.

Source page: https://510kreport.com/device/K101838
Methodology: https://510kreport.com/methodology