# K971549: VMT System

- Pathway: 510(k) (Traditional)
- Applicant: Target Health, Inc.
- Decided: Oct 5, 1998 after 525 days
- Product code: LXV (Apparatus, Vestibular Analysis)
- Device class: U
- 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 K851744 (1985). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K851744: Equitest, Neurocom International, Inc. (1985) Summary page 2.
- K946229: Balance Manager, Neurocom International, Inc. (1995) Summary page 2.

## Indications for use
The VMT™ System is designed for the evaluation of visuo-motor performance disturbances.

Source page: https://510kreport.com/device/K971549
Methodology: https://510kreport.com/methodology