# K984401: Neuromag Vectorview

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems (Cleveland), Inc.
- Decided: Dec 30, 1998 after 21 days
- Product code: OLX (Source Localization Software For Electroencephalograph Or Magnetoencephalograph)
- Device class: 2
- Regulation: 21 CFR 882.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K901215 (1990). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962764: Neuromag-122, Philips Medical Systems (Cleveland), Inc. (1996) Summary page 2.

## Indications for use
The Vectorview is intended for use as a magneto encephalographic (MEG) device which non-invasively detects and displays biomagnetic signals produced by electrically active nerve tissue in the brain. When interpreted by a trained clinician, the data enhances the diagnostic capability by providing useful information about the location relative to brain anatomy of active nerve tissue responsible for critical brain functions.

Source page: https://510kreport.com/device/K984401
Methodology: https://510kreport.com/methodology