FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

THEOPHYLLINE ENZYME IMMUNOASSAY

K Number: K952596 · Decision Aug 11, 1995
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
70
Applicant Total
66
Review Days
66

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Basic Information

Device Name
THEOPHYLLINE ENZYME IMMUNOASSAY
K Number
K952596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3880
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Reagents, Inc.
Date Received
June 6, 1995
Decision Date
August 11, 1995
Product Code
KLS
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KLS Enzyme Immunoassay, Theophylline

Similar 510(k) Clearances

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Other Clearances by Diagnostic Reagents, Inc.

K Number Device Name
K983268 MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY
K983812 NAPA EIA ASSAY
K983323 DIGOXIN IMMUNOASSAY
K983280 VANCOMYCIN EIA ASSAY
K983159 DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLS
K973102 LIDOCAINE EIA ASSAY
K972835 50NG/ML COCAINE METABOLITE CALIBRATOR
K972526 METHADONE EIA ASSAY
K964212 QUINIDINE ENZYME IMMUNOASSAY
K963835 DIGOXIN ENZYME IMMUNOASSAY
Search all 66 clearances from Diagnostic Reagents, Inc. →