# K033821: Kodak Dryview 8900 Laser Imager Mammography Accessory

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Feb 20, 2004 after 73 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 K002146 (2000). 1 ancestor in all.
4 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002146: Kodak Dryview 8610 Laser Imager / for Mammography, Eastman Kodak Company (2000) Summary page 1.

## Most influential descendants
- K042133: Dry Laser Imager, Model  Drypro Model 793 (2004), 2 descendants of its own
- K090469: Carestream Dryview 5850 Laser Imager (2009), 0 descendants of its own
- 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 KODAK DRYVIEW 8900 Laser Imager with Mammography Accessory is intended to provide high-resolution hard copy images from digital imaging source output signals. The device is intended for use with KODAK DRYVIEW DVM film for use with a variety of digital modalities, including, but not limited to, CR (Computed Radiology), DR (Digital Radiology) and FFDM (Full Field Digital mammography). The images are to be used for medical diagnosis medical and referring physicians and their patients.

Source page: https://510kreport.com/device/K033821
Methodology: https://510kreport.com/methodology