# K042133: Dry Laser Imager, Model  Drypro Model 793

- Pathway: 510(k) (Traditional)
- Applicant: Konica Minolta Medical & Graphic, Inc.
- Decided: Nov 24, 2004 after 107 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: 2 generations back to K002146 (2000). 2 ancestors in all.
2 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)
- K033821: Kodak Dryview 8900 Laser Imager Mammography Accessory, Eastman Kodak Company (2004) Summary page 2.

## Most influential descendants
- K083522: Sony UP-DF750 Digital Film Imager (2009), 0 descendants of its own
- K081637: Laser Imager Drypro Model 873 (2008), 0 descendants of its own

## Indications for use
The Dry Laser Imager, DRYPRO Model 793 is intended to be used to acquire images from diagnostic equipment such as CT, MRI, DSA or FDA-approved Full Field Digital Mammography System and print the images on medical dry-film. The devices are intended to be used by trained medical personnel in a clinic or hospital environment.

Source page: https://510kreport.com/device/K042133
Methodology: https://510kreport.com/methodology