Syva Emit II Plus Amphetamine/Methamphetamine Assay 9C029UL/9C129UL

FDA 510(k) K993982 · Syva Co.

Substantially Equivalent

510(k) numberK993982

Submission

Device name
Syva Emit II Plus Amphetamine/Methamphetamine Assay 9C029UL/9C129UL
Applicant
Syva Co.
San Jose, CA, US
Received
November 24, 1999
Decision date
January 27, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LAF – Gas Chromatography, Methamphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3610
Specialty
Clinical Toxicology

Other 510(k)s with product code LAF

510(k)DeviceApplicantDecision
K203647SEFRIA Methamphetamine Oral Fluid Enzyme ImmunoassayLAF · Traditional Immunalysis Corporation12/22/2021SE
K210212Psychemedics Homogeneous Enzyme Immunoassay for Amphetamines in HairLAF · Traditional Psychemedics Corporation12/15/2021SE
K201442Lin-Zhi International, Inc. (LZI) Methamphetamine Enzyme Immunoassay for Pictus AnalyzersLAF · Traditional Diatron Group07/31/2020SE
K170222Rapid Tox Cup IILAF · Traditional American Bio Medica Corp.08/15/2017SE
K153693Immunalysis Methamphetamine Urine Enzyme Immunoassay, Immunalysis Multi-Drug CalibratorsLAF · Traditional Immunalysis Corporation03/18/2016SE
K142293Rapidfret Oral Fluid Assay for Methamphetamine, Rapidfret Oral Fluid Methamphetamine…LAF · Traditional Biophor Diagnostics, Inc.09/18/2015SE
K150096Healgen MDMA (Ecstacy) Test (Strip, Cassette, Cup, Dip Card), Healgen Phencyclidine Test…LAF · Traditional Healgen Scientific,, LLC03/04/2015SE
K150162First Sign Drug of Abuse Dip Card Test, First Sign Drug of Abuse Cup TestLAF · Traditional W.H.P.M., Inc.02/26/2015SE
K133047Rapidfret Oral Fluid Assay for Mdma, Rapidfret Oral Fluid Calibrators, Rapidfret Oral…LAF · Traditional Biophor Diagnostics, Inc.12/18/2014SE
K131652Lzi Oral Fluid Methamphetamine Enzyme Immunoassay, Calibrators, ControlsLAF · Traditional Lin-Zhi International, Inc.03/21/2014SE

More from Lin-Zhi International, Inc.

510(k)DeviceDecision
K011878Emit (R) Tox Salicylic Assay, Model 7SO19UL, Emit (R) Tox Salicylic Acid Calibrators…DKJ · Traditional 08/13/2001SE
K012257Emit II Plus Monoclonal Amphetamine/Methamphetamine Assay Model OSR9C229DKZ · Special 08/03/2001SE
K011947Emit 2000 Valproic Acid Assay, Model OSR4G229ULLEG · Special 07/02/2001SE
K011528Emit 2000 Phenobarbital Assay, Model OSR4D229DLZ · Special 06/06/2001SE
K011347Emit 2000 Phenytoin Assay, Model 0SR4A229DIP · Special 05/17/2001SE
K993981Syva Emit II Plus Propoxyphene Assay, Models 9G029UL/9G129ULJXN · Traditional 02/01/2000SE
K993980Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULDML · Traditional 02/01/2000SE
K993988Syva Emit II Plus Cocaine Metabolite Assay, Model 9H029ULDIO · Traditional 01/27/2000SE
K993987Syva Emit II Plus Barbiturate Assay, Model 9D029UL/9D129ULKLT · Traditional 01/27/2000SE
K993986Syva Emit II Plus Methaqualone Assay, Model 9Q029UL/9Q129ULKXS · Traditional 01/27/2000SE

Questions and answers

When was Syva Emit II Plus Amphetamine/Methamphetamine Assay 9C029UL/9C129UL cleared by the FDA?

Syva Emit II Plus Amphetamine/Methamphetamine Assay 9C029UL/9C129UL (K993982) received a 510(k) decision of Substantially Equivalent on January 27, 2000, 64 days after the submission was received.

What is the product code of K993982?

The FDA product code is LAF – Gas Chromatography, Methamphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3610.