# K152729: Microperimeter MP-3

- Pathway: 510(k) (Traditional)
- Applicant: Nidek Co., Ltd.
- Decided: Jun 6, 2016 after 258 days
- Product code: HKI (Camera, Ophthalmic, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K941234 (1995). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 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 5.

## Most influential descendants
- K190198: Microperimeter MP-3, Microperimeter MP-3 Type S (2019), 0 descendants of its own

## Indications for use
MP-3 MICROPERIMETER is indicated for use as: Color retinography Fixation examiner Fundus-related microperimetry

Source page: https://510kreport.com/device/K152729
Methodology: https://510kreport.com/methodology