Usdt Phencyclidine (PCP) Assay Column Cat. No. 9000-400

FDA 510(k) K935629 · U.S. Drug Testing, Inc.

Substantially Equivalent

510(k) numberK935629

Submission

Device name
Usdt Phencyclidine (PCP) Assay Column Cat. No. 9000-400
Applicant
U.S. Drug Testing, Inc.
Rancho Cucamonga, CA, US
Received
November 23, 1993
Decision date
April 12, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LCM – Enzyme Immunoassay, Phencyclidine
Device class
Unclassified

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More from Microgenics Corp.

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K940912Usdt Cannabinoid (THC) Assay Column Catalog No. 9000-500LDJ · Traditional 06/02/1994SE
K934693Amphetamine Test SystemDKZ · Traditional 11/22/1993SE
K932318Usdt Opiate Assay Column Catalog No. 9000-200DJG · Traditional 06/15/1993SE
K931227Usdt Flow Immunoassay System, Model 9000KZR · Traditional 05/06/1993SE
K930985Usdt Cocaine/Cocaine Metabol Assay COLUMN,9000-100DIO · Traditional 04/27/1993SE

Questions and answers

When was Usdt Phencyclidine (PCP) Assay Column Cat. No. 9000-400 cleared by the FDA?

Usdt Phencyclidine (PCP) Assay Column Cat. No. 9000-400 (K935629) received a 510(k) decision of Substantially Equivalent on April 12, 1994, 140 days after the submission was received.

What is the product code of K935629?

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