Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Ucp Biosciences, Inc.. It received FDA 510(k) clearance on 2016-05-03 under approval 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. It is manufactured by Ucp Biosciences, Inc.. The 510(k) number is K152908.

When was UCP COMPACT DRUG TESTS approved by the FDA?

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

What company makes UCP COMPACT DRUG TESTS?

UCP COMPACT DRUG TESTS is manufactured by Ucp Biosciences, Inc..

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

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

Related Clinical Trials

Related Devices (Code: DKZ)

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.