# K092187: Maia, Model 1

- Pathway: 510(k) (Traditional)
- Applicant: Centervue S.P.A.
- Decided: May 27, 2010 after 310 days
- Product code: HPT (Perimeter, Automatic, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 886.1605
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K941234 (1995). 7 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023719: MP-1 Micro Perimeter, Nidek Technologies Srl (2002) Summary page 2.
- K061768: MP-1 Microperimeter, Nidek Technologies Srl (2006) Summary page 2.
- K063378: Cirrus HD-Oct, Model 4000, Carl Zeiss Meditec, Inc. (2007) Summary page 2.

## Most influential descendants
- K133758: Centervue Macular Integrity Assessment (2014), 3 descendants of its own
- K150320: Compass (2015), 1 descendant of its own
- K243504: Maia (AHMACME001) (2025), 0 descendants of its own
- K153181: MAIA (2016), 0 descendants of its own

## Indications for use
The Macular Integrity Assessment (MAIA™) is indicated for measuring macular sensitivity, fixation stability and the locus of fixation, as well as providing infrared retinal imaging. It contains a reference database that is a quantitative tool for the comparison of macular sensitivity to a database of known normal subjects.

Source page: https://510kreport.com/device/K092187
Methodology: https://510kreport.com/methodology