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FDA 510(k)

DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE

K-Number: K111385 · 2012-01-30

ApplicantQubyx Limited
Decision Date2012-01-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE is the device name listed in this FDA 510(k) record. The listed applicant is Qubyx Limited. It received FDA 510(k) clearance on 2012-01-30 under 510(k) number K111385. 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 DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE?

DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE is a medical device that received FDA 510(k) clearance on 2012-01-30. The listed applicant is Qubyx Limited. The 510(k) number is K111385.

When did DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE receive FDA 510(k) clearance?

DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE received FDA 510(k) clearance on 2012-01-30, under 510(k) number K111385.

Who is the listed applicant for DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE?

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

What is the FDA product code for DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE?

The FDA product code for DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE 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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