# K061768: MP-1 Microperimeter

- Pathway: 510(k) (Traditional)
- Applicant: Nidek Technologies Srl
- Decided: Sep 28, 2006 after 97 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). 5 ancestors in all.
27 later devices descend from it; 4 cite it directly.
0 of 33 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 3.
- K810880: AR-1 Physiological Prodessor, Atlas Researches, Ltd. (1981) Summary page 3.

## Most influential descendants
- K070231: ORION (2007), 22 descendants of its own
- K101935: Centervue Digital Retinography System (2010), 21 descendants of its own
- K142047: EIDON (2014), 8 descendants of its own
- K122572: Icam Fundus Camera (2013), 8 descendants of its own
- K092187: Maia, Model 1 (2010), 4 descendants of its own

## Indications for use
The MP-1 MICRO PERIMETER is indicated for use as: · Color retinography * Fixation examiner * Fundus-relatedmicroperimetry * Visual rehabilitation.

Source page: https://510kreport.com/device/K061768
Methodology: https://510kreport.com/methodology