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FDA 510(k)

CORONIS 2MP-21 AND MFGD 2621

K-Number: K052403 · 2005-09-15

ApplicantBarcoview
Decision Date2005-09-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORONIS 2MP-21 AND MFGD 2621 is the device name listed in this FDA 510(k) record. The listed applicant is Barcoview. It received FDA 510(k) clearance on 2005-09-15 under 510(k) number K052403. 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 2MP-21 AND MFGD 2621?

CORONIS 2MP-21 AND MFGD 2621 is a medical device that received FDA 510(k) clearance on 2005-09-15. The listed applicant is Barcoview. The 510(k) number is K052403.

When did CORONIS 2MP-21 AND MFGD 2621 receive FDA 510(k) clearance?

CORONIS 2MP-21 AND MFGD 2621 received FDA 510(k) clearance on 2005-09-15, under 510(k) number K052403.

Who is the listed applicant for CORONIS 2MP-21 AND MFGD 2621?

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 2MP-21 AND MFGD 2621?

The FDA product code for CORONIS 2MP-21 AND MFGD 2621 is LLZ.

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Related Devices (Code: 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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