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

AIA-PACK TGAB ASSAY

K Number: K981522 · Decision Oct 8, 1998
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
41
Review Days
163

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Basic Information

Device Name
AIA-PACK TGAB ASSAY
K Number
K981522
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tosoh Medics, Inc.
Date Received
April 28, 1998
Decision Date
October 8, 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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K020489 G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE
K012820 AIA-PACK CTNI 2ND-GEN ASSAY
K011434 G7 AUTOMATED HPLC ANALYZER
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K992365 AIA-PACK FOLATE ASSAY
K990431 AIA-PACK CA 125
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