# K071250: CA, Model: Cam

- Pathway: 510(k) (Traditional)
- Applicant: Optovue, Inc.
- Decided: Sep 28, 2007 after 147 days
- Product code: OBO (Tomography, Optical Coherence)
- 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: 4 generations back to K012727 (2002). 6 ancestors in all.
64 later devices descend from it; 5 cite it directly.
0 of 71 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062552: RTVUE, Optovue, Inc. (2006) Summary page 1.
- K051789: Visante Oct, Carl Zeiss Meditec, Inc. (2005) Summary page 1.
- K063343: Bioptigen Spectral Domain Ophthalmic Imaging System, Bioptigen, Inc. (2006) Summary page 1.

## Most influential descendants
- K101505: Rtvue Model Rtvue 100 (2010), 58 descendants of its own
- K111157: CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and GANGLION CELL NORMATIVE DATABASES (2012), 24 descendants of its own
- K120238: Rtvue XR Oct (2012), 17 descendants of its own
- K153080: RTVue XR OCT Avanti with AngioVue Software (2016), 16 descendants of its own
- K091404: Ivue, Model 100 (2010), 16 descendants of its own

## Indications for use
The CA, an auxiliary lens adapter, when used in conjunction with RTVue, is indicated for in vivo imaging and measurement of the cornea and other ocular structures of the anterior segment of the eye.

Source page: https://510kreport.com/device/K071250
Methodology: https://510kreport.com/methodology