# K002146: Kodak Dryview 8610 Laser Imager / for Mammography

- Pathway: 510(k) (Traditional)
- Applicant: Eastman Kodak Company
- Decided: Sep 27, 2000 after 72 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.
14 later devices descend from it; 3 cite it directly.
0 of 15 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
- K012941: Drystar, Model 4500M (2001), 8 descendants of its own
- K021054: Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon GS Medical Multimedia Grey Scale Dry Imager (2002), 6 descendants of its own
- K033821: Kodak Dryview 8900 Laser Imager Mammography Accessory (2004), 4 descendants of its own
- K042133: Dry Laser Imager, Model  Drypro Model 793 (2004), 2 descendants of its own
- K060440: Codonics Horizon XL Digital Direct Long Film Imager; Codonics Horizon XL-X Long Film Imager (2006), 1 descendant of its own

Source page: https://510kreport.com/device/K002146
Methodology: https://510kreport.com/methodology