# K974207: Philips Easyvision Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems North America, Inc.
- Decided: Jan 22, 1998 after 73 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.
No later device cites it as a predicate yet.
0 of 1 device 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 Easyvision Workstation: named in the summary without a submission number

## Indications for use
EasyCorrect is intended for use in situations where digital images acquired from fluoroscopic imaging systems are desired or required without distortion. The corrected images may be either hard-copy or soft-copy.

Source page: https://510kreport.com/device/K974207
Methodology: https://510kreport.com/methodology