# K993708: Biomagnetic Technologies Magnes 3600 Whole Head Meg

- Pathway: 510(k) (Special)
- Applicant: Biomagnetic Technologies, Inc.
- Decided: Dec 3, 1999 after 30 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
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) Magnes® 2500 WH MEG: named in the summary without a submission number

## Indications for use
The Magnes®3600 WH MEG is intended for use in diagnostic procedures that require the measurement and display of extracranial magnetic fields and information about the electrical activity in the brain as inferred from those fields.

Source page: https://510kreport.com/device/K993708
Methodology: https://510kreport.com/methodology