# K111988: Easyscan Model 1.2

- Pathway: 510(k) (Traditional)
- Applicant: I-Optics BV
- Decided: Oct 28, 2011 after 107 days
- Product code: MYC (Ophthalmoscope, Laser, Scanning)
- 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
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K142047: EIDON (2014), 8 descendants of its own
- K180526: Eidon FA (2018), 2 descendants of its own
- K211328: Eidon FA, Eidon, Eidon AF, Eidon Uwfl (2021), 1 descendant of its own
- K192113: DRSplus (2019), 1 descendant of its own
- K150320: Compass (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K111988
Methodology: https://510kreport.com/methodology