# K070270: Piccolight E50,Piccolight E56,Eurolight E10, Eurolight E30, and Eurolight E36

- Pathway: 510(k) (Traditional)
- Applicant: Kirchner & Wilhelm GmbH + Co.Kg
- Decided: Nov 5, 2007 after 280 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: 1 generation back to K925757 (1993). 3 ancestors in all.
4 later devices descend from it; 1 cites 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)
- K925756: UNI II, Rudolf Riester GmbH & Co. KG (1993) Summary page 1.
- K932503: RI-Mini, Rudolf Riester GmbH & Co. KG (1993) Summary page 1.
- K925757: Ophthalmoscope, Rudolf Riester GmbH & Co. KG (1993) Summary page 2.
- (no number) HEINE BETA 200 S ophthalmoscope: named in the summary without a submission number

## Most influential descendants
- K123587: Heine Mini 3000 Led Ophthalmoscope (2013), 3 descendants of its own
- 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
An ophthalmoscope is intended to be used to examine the cornea, aqueous, lens, vitreous and retina of the eye.

Source page: https://510kreport.com/device/K070270
Methodology: https://510kreport.com/methodology