# K083771: Retcam Portable Ophthalmic Imaging System, Model RCP

- Pathway: 510(k) (Special)
- Applicant: Clarity Medical Systems
- Decided: Jan 30, 2009 after 43 days
- Product code: HKI (Camera, Ophthalmic, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1120
- 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 K081858 (2008). 1 ancestor in all.
8 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)
- K081858: Retcam 3 Ophthalmic Imaging System, Clarity Medical Systems (2008) Summary page 1.

## Most influential descendants
- K090326: Ret Cam II, Retcam 3 and Retcam Shuttle and Portable Ophthalmic Imaging Systems (2009), 7 descendants of its own
- K102859: Retcam 3 Opthalmic Imaging System (2011), 4 descendants of its own
- K170527: Phoenix Clinical ICON (2017), 3 descendants of its own
- K183059: 3nethra neo (2018), 1 descendant of its own
- K182263: RetCam 3 ; RetCam Shuttle ; RetCam Portable (2018), 1 descendant of its own

## Indications for use
The RetCam Portable Ophthalmic Imaging System is indicated for general ophthalmic imaging including retinal, corneal and external imaging.

Source page: https://510kreport.com/device/K083771
Methodology: https://510kreport.com/methodology