# K060424: Panoramic, Model 200MA

- Pathway: 510(k) (Special)
- Applicant: Optos Plc.
- Decided: Mar 17, 2006 after 28 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: 3 generations back to K871268 (1987). 6 ancestors in all.
8 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042001: Panoramic 200A, Optos Plc. (2004) Summary page 3.

## Most influential descendants
- K102492: P200MAAF (2010), 7 descendants of its own
- 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

## Indications for use
This device is indicated for use as a wide field and retinal fluorescence imaging ophthalmoscope to aid in the diagnosis and monitoring of diseases or disorders that manifest themselves in the retina.

Source page: https://510kreport.com/device/K060424
Methodology: https://510kreport.com/methodology