LCD MONITOR, RADIFORCE G11, G31, G51
K-Number: K032026 · 2003-08-27
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Device Summary
Frequently Asked Questions
What is the LCD MONITOR, RADIFORCE G11, G31, G51?
LCD MONITOR, RADIFORCE G11, G31, G51 is a medical device that received FDA 510(k) clearance on 2003-08-27. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K032026.
When did LCD MONITOR, RADIFORCE G11, G31, G51 receive FDA 510(k) clearance?
LCD MONITOR, RADIFORCE G11, G31, G51 received FDA 510(k) clearance on 2003-08-27, under 510(k) number K032026.
Who is the listed applicant for LCD MONITOR, RADIFORCE G11, G31, G51?
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 LCD MONITOR, RADIFORCE G11, G31, G51?
The FDA product code for LCD MONITOR, RADIFORCE G11, G31, G51 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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