# K946229: Balance Manager

- Pathway: 510(k) (Traditional)
- Applicant: Neurocom International, Inc.
- Decided: Aug 4, 1995 after 225 days
- Product code: KHX (Platform, Force-Measuring)
- Device class: 1
- Regulation: 21 CFR 890.1575
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K070085: Balance Rehabilitation Unit (Bru) (2007), 5 descendants of its own
- K071973: Epley Omniax (2008), 3 descendants of its own
- K220231: GyroStim (2022), 0 descendants of its own
- K192652: TRV (2020), 0 descendants of its own
- K082634: Vertigone BPPV Goggle (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K946229
Methodology: https://510kreport.com/methodology
