QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA
K-Number: K062929 · 2006-12-18
Advertisement
Device Summary
Frequently Asked Questions
What is the QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA?
QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA is a medical device that received FDA 510(k) clearance on 2006-12-18. The listed applicant is Quest Diagnostics, Inc.. The 510(k) number is K062929.
When did QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA receive FDA 510(k) clearance?
QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA received FDA 510(k) clearance on 2006-12-18, under 510(k) number K062929.
Who is the listed applicant for QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA?
The FDA 510(k) record lists Quest Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA?
The FDA product code for QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA is DIO.
Related Clinical Trials
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.
Other records listing Quest Diagnostics, Inc. as applicant
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.
Related Devices (Code: DIO)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement