510(k) K850920

Device
Emit D.a.u. Propoxyphene Assay
Applicant
SYVA CO.
510(k) number
K850920
Product code
JXN
Decision
Substantially Equivalent (SESE)
Decision date
1985-04-02
Date received
1985-03-05
Regulation
862.3700
Classification name
Enzyme Immunoassay, Propoxyphene
Medical specialty
Clinical Toxicology
Review panel
Clinical Toxicology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JOAN KURJIAN
Address
900 Arastradero Rd. P.O. Box 10058 Palo Alto CA US 94303 94303

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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K022915INSTANT-VIEW PROPOXYPHENE (PPX) URINE TESTAlfa Scientific Designs, Inc.2002-11-29
K020787VERDICT-II PROPOXYPHENEMedtox Diagnostics, Inc.2002-05-02
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K011163MODIFICATION TO THE EMIT II PLUS PROPOXYPHENE ASSAY, MODEL OSR9G229Syva Co., Dade Behring, Inc.2001-05-10
K993981SYVA EMIT II PLUS PROPOXYPHENE ASSAY, MODELS 9G029UL/9G129ULSyva Co.2000-02-01
K983700MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENERoche Diagnostic Systems, Inc.1998-12-11
K955675SYNCHRON SYSTEMS PROPOXYPHENE REAGENTBeckman Instruments, Inc.1996-02-09
K951133CEDIA DAU PROPOXYPHENE ASSAYMicrogenics Corp.1995-05-02