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FDA 510(k)

QUICK UP

K-Number: K110440 · 2011-05-04

ApplicantVoco GmbH
Decision Date2011-05-04
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

QUICK UP is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2011-05-04 under 510(k) number K110440. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK UP?

QUICK UP is a medical device that received FDA 510(k) clearance on 2011-05-04. The listed applicant is Voco GmbH. The 510(k) number is K110440.

When did QUICK UP receive FDA 510(k) clearance?

QUICK UP received FDA 510(k) clearance on 2011-05-04, under 510(k) number K110440.

Who is the listed applicant for QUICK UP?

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

What is the FDA product code for QUICK UP?

The FDA product code for QUICK UP is EBI.

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Related Devices (Code: EBI)

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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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