Milenia(Tm) PCP

FDA 510(k) K902960 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK902960

Submission

Device name
Milenia(Tm) PCP
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
July 5, 1990
Decision date
August 17, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCM – Enzyme Immunoassay, Phencyclidine
Device class
Unclassified

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K131181Omega Laboratories Hair Drug Screening Assay PhencyclidineLCM · Traditional Omega Laboratories, Inc.06/25/2013SE
K122703Rapidfret Oral Fluid Assay for PCP, PCP Calibrator Set, PCP Control Set and Rapidease…LCM · Traditional Biophor Diagnostics, Inc.04/25/2013SE
K111928Psychemedics Phencyclidine EiaLCM · Traditional Psychemedics Corp.05/01/2012SE
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Questions and answers

When was Milenia(Tm) PCP cleared by the FDA?

Milenia(Tm) PCP (K902960) received a 510(k) decision of Substantially Equivalent on August 17, 1990, 43 days after the submission was received.

What is the product code of K902960?

The FDA product code is LCM – Enzyme Immunoassay, Phencyclidine, a Unclassified device.