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Company · US

Electrical Geodesics, Incorporated

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2014. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GWQ	Full-Montage Standard Electroencephalograph	4
OLT	Non-Normalizing Quantitative Electroencephalograph Software	2
OLX	Source Localization Software For Electroencephalograph Or Magnetoencephalograph	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Feb 12, 2014	K131882	GEODESICEEG SYSTEM 400 SERIES (GES 400) Electrical Geodesics, Inc.	OLT
Feb 17, 2012	K112353	GEODESIC EEG MOBILE 100 (GEM 100) Electrical Geodesics, Inc.	GWQ
Dec 21, 2010	K092844	GEOSOURCE Electrical Geodesics, Inc.	OLX
Jan 25, 2007	K063797	GEODESIC EEG SYSTEM 300 Electrical Geodesics, Incorporated	OLT
Jan 26, 2005	K043309	GEODESIC PHOTOGRAMMETRY SYSTEM Electrical Geodesics, Incorporated	GWQ
Aug 4, 2004	K033399	GEODESIC EEG SYSTEM SERIES 100 Electrical Geodesics, Incorporated	GWQ
Sep 19, 2001	K012079	GEODESIC EEG SYSTEM, MODEL 200 Electrical Geodesics, Incorporated	GWQ

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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