Phencyclidine Eia Assay

FDA 510(k) K935320 · Diagnostic Reagents, Inc.

Substantially Equivalent

510(k) numberK935320

Submission

Device name
Phencyclidine Eia Assay
Applicant
Diagnostic Reagents, Inc.
Mountain View, CA, US
Received
October 14, 1993
Decision date
December 29, 1993
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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K983268Modification of Tricyclic Serum Tox Eia AssayLFH · Traditional 11/18/1998SE
K983812Napa Eia AssayLAN · Traditional 11/16/1998SE
K983323Digoxin ImmunoassayKXT · Traditional 11/12/1998SE
K983280Vancomycin Eia AssayLEH · Traditional 11/06/1998SE
K983159Drugs of Abuse Urine Calibrators and ControlsDKB · Traditional 11/05/1998SE
K973102Lidocaine Eia AssayKLR · Traditional 09/12/1997SE
K97283550NG/ML Cocaine Metabolite CalibratorDLJ · Traditional 08/28/1997SE
K972526Methadone Eia AssayDJR · Traditional 08/04/1997SE
K964212Quinidine Enzyme ImmunoassayLBZ · Traditional 12/18/1996SE
K963835Digoxin Enzyme ImmunoassayKXT · Traditional 12/10/1996SE

Questions and answers

When was Phencyclidine Eia Assay cleared by the FDA?

Phencyclidine Eia Assay (K935320) received a 510(k) decision of Substantially Equivalent on December 29, 1993, 76 days after the submission was received.

What is the product code of K935320?

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