Aca Urine Drugs of Abuse Calibrator

FDA 510(k) K872392 · E.I. Dupont DE Nemours & Co., Inc.

Substantially Equivalent

510(k) numberK872392

Submission

Device name
Aca Urine Drugs of Abuse Calibrator
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Wilmington, DE, US
Received
June 19, 1987
Decision date
September 14, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Aca Urine Drugs of Abuse Calibrator cleared by the FDA?

Aca Urine Drugs of Abuse Calibrator (K872392) received a 510(k) decision of Substantially Equivalent on September 14, 1987, 87 days after the submission was received.

What is the product code of K872392?

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