BARBITURATE SERUM TOX EIA ASSAY

Enzyme Immunoassay, Barbiturate

DIAGNOSTIC REAGENTS, INC.

The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for Barbiturate Serum Tox Eia Assay.

Pre-market Notification Details

Device IDK960664
510k NumberK960664
Device Name:BARBITURATE SERUM TOX EIA ASSAY
ClassificationEnzyme Immunoassay, Barbiturate
Applicant DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale,  CA  94086
ContactYug-geng Tsay, Ph.d.
CorrespondentYug-geng Tsay, Ph.d.
DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale,  CA  94086
Product CodeDIS  
CFR Regulation Number862.3150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-02-16
Decision Date1996-05-06

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00380740005573 K960664 000
00630414526911 K960664 000
00884883005587 K960664 000

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.