# K043309: Geodesic Photogrammetry System

- Pathway: 510(k) (Traditional)
- Applicant: Electrical Geodesics, Incorporated
- Decided: Jan 26, 2005 after 56 days
- Product code: GWQ (Full-Montage Standard Electroencephalograph)
- 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) Surgical cameras used as recording accessories to surgical procedures: named in the summary without a submission number

## Indications for use
The Geodesic Photogrammetry System is intended for use in recording precise locations of EEG electrodes in the Geodesic Sensor Net on a patient’s head.

Source page: https://510kreport.com/device/K043309
Methodology: https://510kreport.com/methodology