# K023719: MP-1 Micro Perimeter

- Pathway: 510(k) (Traditional)
- Applicant: Nidek Technologies Srl
- Decided: Dec 23, 2002 after 48 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: 3 generations back to K941234 (1995). 3 ancestors in all.
30 later devices descend from it; 5 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014274: Non-Mydriatic Fundus Camera, Model NM-1000, Nidek, Inc. (2002)
- (no number) Humphrey Field Analyzer: named in the summary without a submission number
- (no number) Confoscan 2 Confocal Microscope: named in the summary without a submission number

## Most influential descendants
- K061768: MP-1 Microperimeter (2006), 27 descendants of its own
- 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

## Indications for use
The MP-1 MICRO PERIMETER is indicated for use as Color retinography Fixation examiner Fundus-related microperimetry

Source page: https://510kreport.com/device/K023719
Methodology: https://510kreport.com/methodology