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FDA 510(k)

QbCheck

K-Number: K143468 · 2016-03-22

ApplicantQbtech AB
Decision Date2016-03-22
Product CodeLQD
DecisionSubstantially Equivalent

Device Summary

QbCheck is the device name listed in this FDA 510(k) record. The listed applicant is Qbtech AB. It received FDA 510(k) clearance on 2016-03-22 under 510(k) number K143468. The device is classified under product code LQD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QbCheck?

QbCheck is a medical device that received FDA 510(k) clearance on 2016-03-22. The listed applicant is Qbtech AB. The 510(k) number is K143468.

When did QbCheck receive FDA 510(k) clearance?

QbCheck received FDA 510(k) clearance on 2016-03-22, under 510(k) number K143468.

Who is the listed applicant for QbCheck?

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

What is the FDA product code for QbCheck?

The FDA product code for QbCheck is LQD.

Related Devices (Code: LQD)

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.

K173915Test of Variables of Attention (T.O.V.A.)The Tova CompanyK170082Test of Variables of Attention (T.O.V.A.) Version 9.0The Tova Company

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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