# K990329: Philips Easyvision Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems North America, Inc.
- Decided: Dec 7, 1999 after 308 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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 Easyvision Workstation: named in the summary without a submission number
- (no number) GE Advantage Windows (Functool) Workstation: named in the summary without a submission number

## Most influential descendants
- K081262: DC Neuro (2008), 2 descendants of its own
- K113701: Visia Neuro (2012), 1 descendant of its own
- K141514: Synapse 3D Tensor Analysis (2014), 0 descendants of its own

## Indications for use
The BOLD Analysis option for the EasyVision is intended for use in analyzing images created using the BOLD function of a Gyroscan NT system. The BOLD Analysis option is useful in quantifying small susceptibility changes in the human brain, created by the execution of specific tasks.

Source page: https://510kreport.com/device/K990329
Methodology: https://510kreport.com/methodology