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

GLIADIN IGA ANTIBODY EIA DETECTION SYSTEM

K Number: K002169 · Decision Oct 19, 2000
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
41
Applicant Total
14
Review Days
93

Basic Information

Device Name
GLIADIN IGA ANTIBODY EIA DETECTION SYSTEM
K Number
K002169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5750
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SCIMEDX CORP.
Date Received
July 18, 2000
Decision Date
October 19, 2000
Product Code
MST
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
MST Antibodies, Gliadin

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K Number Device Name
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K010287 SCIMEDX PHASE II PR3 IGG ANTIBODY EIA
K010289 SCIMEDX PHASE II MPO IGG ANTIBODY EIA
K002189 GLIADIN IGG ANTIBODY EIA DETECTION SYSTEM
K002107 IFA KIT FOR THE DETECTION OF ENDOMYSIAL IGA ANIBODIES USING PRIMATE UMBILICAL CORD (PUC)-EMA/PUC LGA.
K994379 EU-TTG IGA ELISA
K970198 IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES
K962360 IFA KIT FOR THE DETECTION OF C-ANCA ANTIBODIES
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