# K932503: RI-Mini

- Pathway: 510(k) (Traditional)
- Applicant: Rudolf Riester GmbH & Co. KG
- Decided: Oct 8, 1993 after 140 days
- Product code: ERA (Otoscope)
- Device class: 1
- Regulation: 21 CFR 874.4770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K070270: Piccolight E50,Piccolight E56,Eurolight E10, Eurolight E30, and Eurolight E36 (2007), 4 descendants of its own
- 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

Source page: https://510kreport.com/device/K932503
Methodology: https://510kreport.com/methodology