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FDA 510(k)

COLOR NIO 2MP, E-2320 C

K-Number: K052958 · 2005-11-16

ApplicantBarcoview
Decision Date2005-11-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLOR NIO 2MP, E-2320 C is the device name listed in this FDA 510(k) record. The listed applicant is Barcoview. It received FDA 510(k) clearance on 2005-11-16 under 510(k) number K052958. 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 COLOR NIO 2MP, E-2320 C?

COLOR NIO 2MP, E-2320 C is a medical device that received FDA 510(k) clearance on 2005-11-16. The listed applicant is Barcoview. The 510(k) number is K052958.

When did COLOR NIO 2MP, E-2320 C receive FDA 510(k) clearance?

COLOR NIO 2MP, E-2320 C received FDA 510(k) clearance on 2005-11-16, under 510(k) number K052958.

Who is the listed applicant for COLOR NIO 2MP, E-2320 C?

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

What is the FDA product code for COLOR NIO 2MP, E-2320 C?

The FDA product code for COLOR NIO 2MP, E-2320 C 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 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.

View all 17 devices →

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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