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FDA 510(k)

AXIS-V MONOCHROME 5 MP DISPLAY

K-Number: K063066 · 2007-08-03

ApplicantNational Display Systems
Decision Date2007-08-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AXIS-V MONOCHROME 5 MP DISPLAY is the device name listed in this FDA 510(k) record. The listed applicant is National Display Systems. It received FDA 510(k) clearance on 2007-08-03 under 510(k) number K063066. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIS-V MONOCHROME 5 MP DISPLAY?

AXIS-V MONOCHROME 5 MP DISPLAY is a medical device that received FDA 510(k) clearance on 2007-08-03. The listed applicant is National Display Systems. The 510(k) number is K063066.

When did AXIS-V MONOCHROME 5 MP DISPLAY receive FDA 510(k) clearance?

AXIS-V MONOCHROME 5 MP DISPLAY received FDA 510(k) clearance on 2007-08-03, under 510(k) number K063066.

Who is the listed applicant for AXIS-V MONOCHROME 5 MP DISPLAY?

The FDA 510(k) record lists National Display Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AXIS-V MONOCHROME 5 MP DISPLAY?

The FDA product code for AXIS-V MONOCHROME 5 MP DISPLAY 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.

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Other records listing National Display Systems 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.

K042353AXIS I (1MP), II (2MP), III (3MP), AND V (5MP) MONOCHROME DISPLAYSK040310NOVA FAMILY OF MEDICAL RADIOLOGY DISPLAYS

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.

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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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