# K945475: Fuji Medical Laser Imager FL-IM D

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Mar 9, 1995 after 121 days
- Product code: LMC (Camera, Multi Format, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K962967: Fuji Medical Dry Imager FM-DP 2636 (1996), 2 descendants of its own
- K024188: UP-DF500 Filmstation Digital Film Imager (2003), 1 descendant of its own
- K083522: Sony UP-DF750 Digital Film Imager (2009), 0 descendants of its own
- K972660: Raven Dry Printer (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K945475
Methodology: https://510kreport.com/methodology