# K911795: Kinesthetic Ability Trainer (K.a.T., Model 1000)

- Pathway: 510(k) (Traditional)
- Applicant: Breg, Inc.
- Decided: Nov 19, 1991 after 211 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
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K070676: Korebalance (Kinesthetic Ability Trainer) (2007), 5 descendants of its own
- K121590: Vestibular Analysis Apparatus (2012), 3 descendants of its own
- K183661: ClearEdge Balance System (2019), 0 descendants of its own
- K190735: EQ Balance (2019), 0 descendants of its own
- K173669: K-D Balance (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K911795
Methodology: https://510kreport.com/methodology