# K052268: Visucam Pro NM

- Pathway: 510(k) (Special)
- Applicant: Carl Zeiss Meditec, AG
- Decided: Nov 2, 2005 after 75 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: 3 generations back to K941234 (1995). 5 ancestors in all.
21 later devices descend from it; 3 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043222: Viscucam C Digital Camera, Carl Zeiss Meditec, AG (2005) Summary page 1.

## Most influential descendants
- K112184: Cirrus Photo (2012), 13 descendants of its own
- K141844: Rescan 700, Callisto Eye (2014), 5 descendants of its own
- K150467: Retina Workplace (2015), 3 descendants of its own
- K133217: Cirrus Photo (2014), 3 descendants of its own
- K091064: Navilas Laser System (2009), 3 descendants of its own

## Indications for use
The VISUCAM PRO NM Digital Camera is suitable for photographing, displaying and storing the data of the retina and surrounding parts of the eye to be examined under mydriatic and non-mydriatic conditions. These photographs support the diagnosis and subsequent observation of eye diseases which can be visually monitored and photographically documented.

Source page: https://510kreport.com/device/K052268
Methodology: https://510kreport.com/methodology