MONOCHROME LCD MONITOR, RADIFORCE, GS320
K-Number: K062053 · 2006-08-07
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Device Summary
Frequently Asked Questions
What is the MONOCHROME LCD MONITOR, RADIFORCE, GS320?
MONOCHROME LCD MONITOR, RADIFORCE, GS320 is a medical device that received FDA 510(k) clearance on 2006-08-07. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K062053.
When did MONOCHROME LCD MONITOR, RADIFORCE, GS320 receive FDA 510(k) clearance?
MONOCHROME LCD MONITOR, RADIFORCE, GS320 received FDA 510(k) clearance on 2006-08-07, under 510(k) number K062053.
Who is the listed applicant for MONOCHROME LCD MONITOR, RADIFORCE, GS320?
The FDA 510(k) record lists Eizo Nanao Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONOCHROME LCD MONITOR, RADIFORCE, GS320?
The FDA product code for MONOCHROME LCD MONITOR, RADIFORCE, GS320 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 Eizo Nanao Corporation 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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