# K100095: Central Vision Analyzer Model 1000

- Pathway: 510(k) (Abbreviated)
- Applicant: Vimetrics,Llc.
- Decided: May 10, 2010 after 117 days
- Product code: HOX (Chart, Visual Acuity)
- Device class: 1
- Regulation: 21 CFR 886.1150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) ETDRS, 3 meter, logMAR 0.1, Sloan Letter translucent charts (Precision Vision): named in the summary without a submission number

## Most influential descendants
- K220090: Visibly Digital Acuity Product (2022), 0 descendants of its own

## Indications for use
The CVA-1000 is intended for use under the direct supervision of an ophthalmologist or optometrist in the measurement of vision at fixation in one or both eyes, with or without optical correction.

Source page: https://510kreport.com/device/K100095
Methodology: https://510kreport.com/methodology