# K100954: Adapt, Model AX-03SN

- Pathway: 510(k) (Traditional)
- Applicant: Apeliotus Vision Science, Inc.
- Decided: Feb 25, 2011 after 324 days
- Product code: OUM (Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation)
- Device class: 1
- Regulation: 21 CFR 886.1050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) Goldmann-Weekers adaptometer: named in the summary without a submission number

## Indications for use
The AdaptTM is an AC powered, automated adaptometer (biophotometer) intended to measure the time for retinal adaptation after exposure to an adapting light.

Source page: https://510kreport.com/device/K100954
Methodology: https://510kreport.com/methodology