# K973835: Philips Easyvision Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: Jan 6, 1998 after 90 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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. The FDA summary names its predicate without a number.
- (no number) Philips Integris: named in the summary without a submission number
- (no number) Siemens: named in the summary without a submission number

## Most influential descendants
- K153103: CARESTREAM Vue PACS (2016), 0 descendants of its own

## Indications for use
The Vascular Analysis Package is intended for off-line image processing and manipulation of digitally acquired datasets from Integris systems. The use of the Vascular Analysis package is comparable with that on the Integris operator console (the algorithms used with the Easyvision are identical to those already used on the Integris systems, although the user interface is different). With the Vascular Analysis package the user can optimize images and perceived image quality for vascular application specific purposes.

Source page: https://510kreport.com/device/K973835
Methodology: https://510kreport.com/methodology