# K123587: Heine Mini 3000 Led Ophthalmoscope

- Pathway: 510(k) (Abbreviated)
- Applicant: Heine Optotechnik GmbH & Co. KG
- Decided: Mar 22, 2013 after 121 days
- Product code: HLJ (Ophthalmoscope, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K925757 (1993). 4 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070270: Piccolight E50,Piccolight E56,Eurolight E10, Eurolight E30, and Eurolight E36, Kirchner & Wilhelm GmbH + Co.Kg (2007) Summary page 2.

## Most influential descendants
- K142486: Heine Beta 200, Heine Beta 200 S, Heine K 180 (2015), 0 descendants of its own
- K131959: Heine Mini 3000(R) Ophthalmoscope (2014), 0 descendants of its own
- K131961: Heine Beta 200(R) Ophthalmoscope (2013), 0 descendants of its own

## Indications for use
The HEINE mini 3000® LED Ophthalmoscope is a battery powered hand-held device for medical professionals, containing illumination and viewing optics intended to examine the media (cornea, aqueous, lens, vitreous) and the retina of the eye.

Source page: https://510kreport.com/device/K123587
Methodology: https://510kreport.com/methodology