# DEN180008: Wound Autofluorescence Imaging Device

- Pathway: De Novo
- Applicant: unknown
- Decided: —
- Product code: QCR (Wound Autofluorescence Imaging Device)
- Device class: 1
- Regulation: 21 CFR 878.4165
- 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. De Novo decisions do not claim a predicate device.

## Most influential descendants
- K230734: Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009) (2023), 0 descendants of its own

Source page: https://510kreport.com/device/DEN180008
Methodology: https://510kreport.com/methodology