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

THYROID PEROXIDASE AUTO ANTIBODIES(TPO) IMMUN KIT

K Number: K931311 · Decision May 14, 1993
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
15
Review Days
60

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Basic Information

Device Name
THYROID PEROXIDASE AUTO ANTIBODIES(TPO) IMMUN KIT
K Number
K931311
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nichols Institute
Date Received
March 15, 1993
Decision Date
May 14, 1993
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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Other Clearances by Nichols Institute

K Number Device Name
K952559 ERYTHROPOIETIN IMMUNOASSAY KIT
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K946247 IGFBP-3; INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3
K950524 NICHOLS INSTITUTE DIAGNOSTICS DHEA-S CHEMILUMINESCENCE IMMUNOASSAY
K932650 ERYTHROPOIETIN IMMUNOASSAY KIT
K931600 CHEMILUMINESCENCE FREE T3 IMMUNOASSAY
K931777 APO A-1 CHEMILUMINESCENCE ASSAY
K931601 CHEMILUMINESCENCE DHEA-S IMMUNOASSAY
K926396 ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT
K930777 THYROGLOBULIN AUTOANTIBODY IMMUNOASSAY KIT
Search all 15 clearances from Nichols Institute →