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

ANTI-TG IGG ELISA TEST SYSTEM

K Number: K983553 · Decision Dec 7, 1998
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
13
Review Days
59

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Basic Information

Device Name
ANTI-TG IGG ELISA TEST SYSTEM
K Number
K983553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Columbia Bioscience, Inc.
Date Received
October 9, 1998
Decision Date
December 7, 1998
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

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K983605 IS BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM
K983606 IS BORRELIA BURGDORFERI IGM TEST SYSTEM
K982348 EBNA-1 IGM ELISA TEST SYSTEM
K982352 VCA IGM ELISA TEST SYSTEM
K982350 EA-D IGM ELISA TEST SYSTEM
K983740 IS-ANTI-PR3 IGG ELISA TEST SYSTEM
K983390 IS-ANTI-MPO IGG ELISA TEST SYSTEM
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