# K192652: TRV

- Pathway: 510(k) (Traditional)
- Applicant: Interacoustics A/S
- Decided: May 27, 2020 after 246 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: 3 generations back to K946229 (1995). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071973: Epley Omniax, Vesticon (2008) Summary page 4.

## Indications for use
The TRV is intended to assist in the diagnosis and treatment of balance disorders and vertigo, including benign paroxysmal positional vertigo.

Source page: https://510kreport.com/device/K192652
Methodology: https://510kreport.com/methodology