# K902954: OBER2 Monitor, Eye Movement (Ophthalmic)

- Pathway: 510(k) (Traditional)
- Applicant: Permobil AB
- Decided: Aug 23, 1990 after 49 days
- Product code: HFC (Aspirator, Endocervical)
- Device class: 2
- Regulation: 21 CFR 884.1050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K152890: Saccadometer Plus, Saccadometer Advanced (2016), 1 descendant of its own
- K222484: Retitrack (2023), 0 descendants of its own
- K033949: Varilux Visionprint System (VPS) (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K902954
Methodology: https://510kreport.com/methodology