FDA 510(k)

CANNABINOIDS URINE TEST

K-Number: K110182 · 2011-05-20

ApplicantGuangzhou Wondfo Biotech Co., Ltd.

Decision Date2011-05-20

Product CodeLDJ

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

CANNABINOIDS URINE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Wondfo Biotech Co., Ltd.. It received FDA 510(k) clearance on 2011-05-20 under 510(k) number K110182. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNABINOIDS URINE TEST?

CANNABINOIDS URINE TEST is a medical device that received FDA 510(k) clearance on 2011-05-20. The listed applicant is Guangzhou Wondfo Biotech Co., Ltd.. The 510(k) number is K110182.

When did CANNABINOIDS URINE TEST receive FDA 510(k) clearance?

CANNABINOIDS URINE TEST received FDA 510(k) clearance on 2011-05-20, under 510(k) number K110182.

Who is the listed applicant for CANNABINOIDS URINE TEST?

The FDA 510(k) record lists Guangzhou Wondfo Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANNABINOIDS URINE TEST?

The FDA product code for CANNABINOIDS URINE TEST is LDJ.

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Other records listing Guangzhou Wondfo Biotech Co., Ltd. as applicant

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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.