# K134039: Daytona Icg (P200TICG)

- Pathway: 510(k) (Traditional)
- Applicant: Optos Plc.
- Decided: Apr 11, 2014 after 101 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
Longest line of descent: 1 generation back to K971671 (1997). 1 ancestor in all.
6 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)
- K971671: Heidelberg Retina Angiograph FA/Icga (Hra/C), Heidelberg Engineering (1997) Summary page 1.

## Most influential descendants
- K142897: P200DTx (2015), 5 descendants of its own
- K173707: P200TE (2018), 3 descendants of its own
- K231673: P200TE (A10700) (2023), 1 descendant of its own
- K233602: P200TE (A10700) (2024), 0 descendants of its own
- K221320: Scanning Laser Ophthalmoscope Mirante [SLO/OCT Model] with Image Filing Software NAVIS-EX; Scanning Laser Ophthalmoscope Mirante [SLO Model] with Image Filing Software NAVIS-EX (2023), 0 descendants of its own

## Indications for use
The Daytona lOG scanning laser ophthalmoscape is indicated for use as a wide field scanning laser ophthalmoscope for viewing choroidal circulation patterns that are illuminated using indlocyanine green dye and for aiding in born the assessment of choroidal circulation and in the diagnosis of choroiditis or choroidal diseases.

Source page: https://510kreport.com/device/K134039
Methodology: https://510kreport.com/methodology