Modification to the Emit II Plus Phencyclidine Assay, Model OSR9J229

FDA 510(k) K011161 · Syva Co., Dade Behring, Inc.

Substantially Equivalent

510(k) numberK011161

Submission

Device name
Modification to the Emit II Plus Phencyclidine Assay, Model OSR9J229
Applicant
Syva Co., Dade Behring, Inc.
San Jose, CA, US
Received
April 16, 2001
Decision date
May 15, 2001
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary 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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K011300Emit II Plus Cannabinoid Assay, Model OSR9N229LDJ · Special 05/17/2001SE
K011306Emit II Plus Benzodiazepine Assay, Model 0SR9F229JXM · Special 05/16/2001SE
K011289Emit II Plus Opiate Assay, Model OSR9B229DJG · Special 05/15/2001SE
K011166Modification to Emit 2000 Theophylline Assay, Model Osr 4P229KLS · Special 05/10/2001SE
K011164Modification to the Emit II Plus Methaqualone Assay, Model OSR9Q229KXS · Special 05/10/2001SE
K011163Modification to the Emit II Plus Propoxyphene Assay, Model OSR9G229JXN · Special 05/10/2001SE
K011162Modification to the Emit II Plus Cocaine Metabolite AssayDIO · Special 05/02/2001SE

Questions and answers

When was Modification to the Emit II Plus Phencyclidine Assay, Model OSR9J229 cleared by the FDA?

Modification to the Emit II Plus Phencyclidine Assay, Model OSR9J229 (K011161) received a 510(k) decision of Substantially Equivalent on May 15, 2001, 29 days after the submission was received.

What is the product code of K011161?

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