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FDA 510(k)

NIO 5MP DISPLAY, MODEL E5620

K-Number: K072875 · 2008-01-22

Decision Date2008-01-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NIO 5MP DISPLAY, MODEL E5620 is the device name listed in this FDA 510(k) record. The listed applicant is Barcoview, Medical Imaging Systems. It received FDA 510(k) clearance on 2008-01-22 under 510(k) number K072875. 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 NIO 5MP DISPLAY, MODEL E5620?

NIO 5MP DISPLAY, MODEL E5620 is a medical device that received FDA 510(k) clearance on 2008-01-22. The listed applicant is Barcoview, Medical Imaging Systems. The 510(k) number is K072875.

When did NIO 5MP DISPLAY, MODEL E5620 receive FDA 510(k) clearance?

NIO 5MP DISPLAY, MODEL E5620 received FDA 510(k) clearance on 2008-01-22, under 510(k) number K072875.

Who is the listed applicant for NIO 5MP DISPLAY, MODEL E5620?

The FDA 510(k) record lists Barcoview, Medical Imaging Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIO 5MP DISPLAY, MODEL E5620?

The FDA product code for NIO 5MP DISPLAY, MODEL E5620 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 Barcoview, Medical Imaging 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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