GEODESIC PHOTOGRAMMETRY SYSTEM
K-Number: K043309 · 2005-01-26
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Device Summary
Frequently Asked Questions
What is the GEODESIC PHOTOGRAMMETRY SYSTEM?
GEODESIC PHOTOGRAMMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 2005-01-26. The listed applicant is Electrical Geodesics, Incorporated. The 510(k) number is K043309.
When did GEODESIC PHOTOGRAMMETRY SYSTEM receive FDA 510(k) clearance?
GEODESIC PHOTOGRAMMETRY SYSTEM received FDA 510(k) clearance on 2005-01-26, under 510(k) number K043309.
Who is the listed applicant for GEODESIC PHOTOGRAMMETRY SYSTEM?
The FDA 510(k) record lists Electrical Geodesics, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GEODESIC PHOTOGRAMMETRY SYSTEM?
The FDA product code for GEODESIC PHOTOGRAMMETRY SYSTEM is GWQ.
Related Clinical Trials
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.
Other records listing Electrical Geodesics, Incorporated 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.
Related Devices (Code: GWQ)
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.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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