Multiple Analyte Urine Drugs of Abuse Calibrators and Controls

FDA 510(k) K051088 · Lin-Zhi International, Inc.

Substantially Equivalent

510(k) numberK051088

Submission

Device name
Multiple Analyte Urine Drugs of Abuse Calibrators and Controls
Applicant
Lin-Zhi International, Inc.
Synnyvale, CA, US
Received
April 28, 2005
Decision date
June 24, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DKB – Calibrators, Drug Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3200
Specialty
Clinical Toxicology

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Questions and answers

When was Multiple Analyte Urine Drugs of Abuse Calibrators and Controls cleared by the FDA?

Multiple Analyte Urine Drugs of Abuse Calibrators and Controls (K051088) received a 510(k) decision of Substantially Equivalent on June 24, 2005, 57 days after the submission was received.

What is the product code of K051088?

The FDA product code is DKB – Calibrators, Drug Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.3200.