VIATRONIX V3D COLON
K-Number: K020658 · 2002-03-07
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Device Summary
Frequently Asked Questions
What is the VIATRONIX V3D COLON?
VIATRONIX V3D COLON is a medical device that received FDA 510(k) clearance on 2002-03-07. The listed applicant is Viatronix, Inc.. The 510(k) number is K020658.
When did VIATRONIX V3D COLON receive FDA 510(k) clearance?
VIATRONIX V3D COLON received FDA 510(k) clearance on 2002-03-07, under 510(k) number K020658.
Who is the listed applicant for VIATRONIX V3D COLON?
The FDA 510(k) record lists Viatronix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIATRONIX V3D COLON?
The FDA product code for VIATRONIX V3D COLON is LLZ.
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 Viatronix, 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.
Related Devices (Code: LLZ)
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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