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

TPO IGG ANTIBODY EIA TEST

K Number: K011082 · Decision Jun 6, 2001
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
14
Review Days
57

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Basic Information

Device Name
TPO IGG ANTIBODY EIA TEST
K Number
K011082
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Scimedx Corp.
Date Received
April 10, 2001
Decision Date
June 6, 2001
Product Code
JZO
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
JZO System, Test, Thyroid Autoantibody

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JZO), ordered by most recent decision date.

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Other Clearances by Scimedx Corp.

K Number Device Name
K011348 PHASE II GBM IGG ANTIBODY EIA TEST
K010625 EUROSPITAL EU-TTG IGA UMANA
K010287 SCIMEDX PHASE II PR3 IGG ANTIBODY EIA
K010289 SCIMEDX PHASE II MPO IGG ANTIBODY EIA
K002189 GLIADIN IGG ANTIBODY EIA DETECTION SYSTEM
K002169 GLIADIN IGA 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
Search all 14 clearances from Scimedx Corp. →