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FDA 510(k)

UCP COMPACT DRUG TESTS

K-Number: K152908 · 2016-05-03

Decision Date2016-05-03
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

UCP COMPACT DRUG TESTS is the device name listed in this FDA 510(k) record. The listed applicant is Ucp Biosciences, Inc.. It received FDA 510(k) clearance on 2016-05-03 under 510(k) number K152908. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCP COMPACT DRUG TESTS?

UCP COMPACT DRUG TESTS is a medical device that received FDA 510(k) clearance on 2016-05-03. The listed applicant is Ucp Biosciences, Inc.. The 510(k) number is K152908.

When did UCP COMPACT DRUG TESTS receive FDA 510(k) clearance?

UCP COMPACT DRUG TESTS received FDA 510(k) clearance on 2016-05-03, under 510(k) number K152908.

Who is the listed applicant for UCP COMPACT DRUG TESTS?

The FDA 510(k) record lists Ucp Biosciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UCP COMPACT DRUG TESTS?

The FDA product code for UCP COMPACT DRUG TESTS is DKZ.

Related Devices (Code: DKZ)

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.

Official Source

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