# K972660: Raven Dry Printer

- Pathway: 510(k) (Traditional)
- Applicant: Sterling Diagnostic Imaging, Inc.
- Decided: Nov 10, 1997 after 117 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 K912073 (1991). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K912073: Polaroid Helios Laser Imager, Polaroid Medical Corp. (1991) Summary page 1.
- K945475: Fuji Medical Laser Imager FL-IM D, Fujifilm Medical System U.S.A., Inc. (1995) Summary page 1.

## Indications for use
The Raven is a free standing device used to print diagnostic images on a polyester base for viewing on a standard view box and/or print reports and referral quality images on paper. It may be used in any situation in which a hard copy of an image generated by a medical imaging device is required or desirable.

Source page: https://510kreport.com/device/K972660
Methodology: https://510kreport.com/methodology