# K971760: Colorpoint or Professional Colorpoint

- Pathway: 510(k) (Traditional)
- Applicant: Seiko Instruments USA, Inc.
- Decided: Oct 1, 1997 after 142 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.
5 later devices descend from it; 1 cites 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)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K991282: Colorpoint 1720 Medical Imagers and Video Capture Box CX-1000 Series (1999), 4 descendants of its own
- K030690: Codonics EP-1000 Medical Color Dry Imagers (2003), 3 descendants of its own
- K042232: NP-2600 Series Hardcopy Printers (2004), 1 descendant of its own
- K092280: Cypher Dicom Print Solution (2009), 0 descendants of its own
- K042159: Kodak Color Medical Imager 1000 (2004), 0 descendants of its own

## Indications for use
The device is indicated for producing full-bleed thermal wax prints on all media sizes from medical image signal inputs.

Source page: https://510kreport.com/device/K971760
Methodology: https://510kreport.com/methodology