# K992586: Konica Laser Imager, Drypro Model 722

- Pathway: 510(k) (Traditional)
- Applicant: Konica Corp.
- Decided: Oct 29, 1999 after 88 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K013052: Konica Laser Imager, Drypro Model 751/752 (2002), 0 descendants of its own

## Indications for use
The Konica Laser Imager DRYPRO model 722 is a laser imager converts data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

Source page: https://510kreport.com/device/K992586
Methodology: https://510kreport.com/methodology