FDA 510(k)

NIO 5MP, MODEL MDNG-5121

K-Number: K073205 · 2007-12-19

ApplicantBarcoview, Medical Imaging Systems

Decision Date2007-12-19

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

NIO 5MP, MODEL MDNG-5121 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 2007-12-19 under 510(k) number K073205. 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, MODEL MDNG-5121?

NIO 5MP, MODEL MDNG-5121 is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Barcoview, Medical Imaging Systems. The 510(k) number is K073205.

When did NIO 5MP, MODEL MDNG-5121 receive FDA 510(k) clearance?

NIO 5MP, MODEL MDNG-5121 received FDA 510(k) clearance on 2007-12-19, under 510(k) number K073205.

Who is the listed applicant for NIO 5MP, MODEL MDNG-5121?

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, MODEL MDNG-5121?

The FDA product code for NIO 5MP, MODEL MDNG-5121 is LLZ.

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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.