# K162991: YELLOW 560 Fluorescence Module

- Pathway: 510(k) (Traditional)
- Applicant: Carl Zeiss Meditec, AG
- Decided: Jul 24, 2017 after 270 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K231075: Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K162991
Methodology: https://510kreport.com/methodology