# K013052: Konica Laser Imager, Drypro Model 751/752

- Pathway: 510(k) (Traditional)
- Applicant: Konica Minolta Medical & Graphic, Inc.
- Decided: Jan 16, 2002 after 127 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 K992586 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992586: Konica Laser Imager, Drypro Model 722, Konica Corp. (1999) Summary page 2.

## Indications for use
The Konica Laser Imager DRYPRO model 751/752 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/K013052
Methodology: https://510kreport.com/methodology