Milenia Cocaine Metabolite

FDA 510(k) K910044 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK910044

Submission

Device name
Milenia Cocaine Metabolite
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
January 4, 1991
Decision date
February 13, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLN – Radioimmunoassay, Cocaine Metabolite
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3250
Specialty
Clinical Toxicology

Other 510(k)s with product code KLN

510(k)DeviceApplicantDecision
K010868Psychemedics Ria Cocaine AssayKLN · Traditional Psychemedics Corp.11/06/2001SE
K913867Urine Cocaine Metabolite Direct Ria Kit (I-125)KLN · Traditional Immunalysis Corporation09/19/1991SE
K913722Abuscreen(R) Radioimmun for Cocaine MetaboliteKLN · Traditional Roche Diagnostic Systems, Inc.09/10/1991SE
K912756Abuscreen Radioimmunoassay for Cocaine MetaboliteKLN · Traditional Roche Diagnostic Systems, Inc.07/26/1991SE
K910123Target Cocaine Metabolite-VKLN · Traditional V-Tech, Inc.03/19/1991SE
K910122Target Cocaine Metabolite-RKLN · Traditional V-Tech, Inc.03/19/1991SE
K905730Abuscreen Ontrak for Cocaine (200NG/ML)KLN · Traditional Roche Diagnostic Systems, Inc.01/15/1991SE
K904995Abuscreen Online TM for Cocaine MetaboliteKLN · Traditional Roche Diagnostic Systems, Inc.11/28/1990SE
K880674Micromedic Crackpot Ria KitKLN · Traditional Icn Micromedic Systems10/06/1988SE
K871549Resub. Urine Cocaine Meta. Direct Ria Kit [I-125]KLN · Traditional Immunalysis Corporation06/16/1987SE

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Questions and answers

When was Milenia Cocaine Metabolite cleared by the FDA?

Milenia Cocaine Metabolite (K910044) received a 510(k) decision of Substantially Equivalent on February 13, 1991, 40 days after the submission was received.

What is the product code of K910044?

The FDA product code is KLN – Radioimmunoassay, Cocaine Metabolite, a Class II (moderate risk) device regulated under 21 CFR 862.3250.