# K963980: Philips Easyvision

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems North America, Inc.
- Decided: Dec 23, 1996 after 81 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- 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 no predicate by number.

## Most influential descendants
- K992925: AX Workstation DR-Viewer Software Option (1999), 0 descendants of its own

## Recalls of this device
- Mar 10, 2008 · Not classified · Z-2053-2008: Inaccurate measurements when exporting radiography images to Picture Archiving and Communication System (PACS ).

Source page: https://510kreport.com/device/K963980
Methodology: https://510kreport.com/methodology