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FDA 510(k)

GEOSOURCE

K-Number: K092844 · 2010-12-21

ApplicantElectrical Geodesics, Inc.
Decision Date2010-12-21
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GEOSOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Electrical Geodesics, Inc.. It received FDA 510(k) clearance on 2010-12-21 under 510(k) number K092844. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GEOSOURCE?

GEOSOURCE is a medical device that received FDA 510(k) clearance on 2010-12-21. The listed applicant is Electrical Geodesics, Inc.. The 510(k) number is K092844.

When did GEOSOURCE receive FDA 510(k) clearance?

GEOSOURCE received FDA 510(k) clearance on 2010-12-21, under 510(k) number K092844.

Who is the listed applicant for GEOSOURCE?

The FDA 510(k) record lists Electrical Geodesics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GEOSOURCE?

The FDA product code for GEOSOURCE is OLX.

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Other records listing Electrical Geodesics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112353GEODESIC EEG MOBILE 100 (GEM 100)

Related Devices (Code: OLX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260563CN-Suite™FIND Surgical Sciences Inc. D/B/A FIND NeuroK252565PreOp v3Clouds of CareK250239NeuroMatchLVIS CorporationK241513SourcererBrain Electrophysiology Laboratory Company, LLCK233985TRIUX™ neo (NM27000N ); MEGreview (SW26241N-B)Megin OYK210199RICOH MEGRicoh Company, Ltd.

Official Source

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