# K962967: Fuji Medical Dry Imager FM-DP 2636

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Oct 28, 1996 after 90 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
Longest line of descent: 1 generation back to K945475 (1995). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945475: Fuji Medical Laser Imager FL-IM D, Fujifilm Medical System U.S.A., Inc. (1995) Summary page 1.

## Most influential descendants
- 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

## Indications for use
The indications for use of the Fuji Medical Dry Imagers is the production of hard copy images from medical image data.

Source page: https://510kreport.com/device/K962967
Methodology: https://510kreport.com/methodology