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FDA 510(k)

CORONIS COLOR 3MP AND MDCC 3120-DL

K-Number: K061927 · 2006-09-05

ApplicantBarcoview
Decision Date2006-09-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORONIS COLOR 3MP AND MDCC 3120-DL is the device name listed in this FDA 510(k) record. The listed applicant is Barcoview. It received FDA 510(k) clearance on 2006-09-05 under 510(k) number K061927. 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 CORONIS COLOR 3MP AND MDCC 3120-DL?

CORONIS COLOR 3MP AND MDCC 3120-DL is a medical device that received FDA 510(k) clearance on 2006-09-05. The listed applicant is Barcoview. The 510(k) number is K061927.

When did CORONIS COLOR 3MP AND MDCC 3120-DL receive FDA 510(k) clearance?

CORONIS COLOR 3MP AND MDCC 3120-DL received FDA 510(k) clearance on 2006-09-05, under 510(k) number K061927.

Who is the listed applicant for CORONIS COLOR 3MP AND MDCC 3120-DL?

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 CORONIS COLOR 3MP AND MDCC 3120-DL?

The FDA product code for CORONIS COLOR 3MP AND MDCC 3120-DL is LLZ.

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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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