# K161328: Cantab Mobile

- Pathway: 510(k) (Traditional)
- Applicant: Cambridge Cognition, Ltd., US Agent: Clementi Associates, Ltd.
- Decided: Jan 13, 2017 after 246 days
- Product code: PKQ (Computerized Cognitive Assessment Aid)
- Device class: 2
- Regulation: 21 CFR 882.1470
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The CANTAB Mobile is intended to be used as an adjunctive tool to assess memory by testing visuospatial associative learning in patients aged 50 to 90 years.

Source page: https://510kreport.com/device/K161328
Methodology: https://510kreport.com/methodology