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

CHEMILUMINESCENCE FREE T3 IMMUNOASSAY

K Number: K931600 · Decision Sep 8, 1993
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
15
Review Days
160

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Basic Information

Device Name
CHEMILUMINESCENCE FREE T3 IMMUNOASSAY
K Number
K931600
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nichols Institute
Date Received
April 1, 1993
Decision Date
September 8, 1993
Product Code
CDP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CDP Radioimmunoassay, Total Triiodothyronine

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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
K931777 APO A-1 CHEMILUMINESCENCE ASSAY
K931601 CHEMILUMINESCENCE DHEA-S IMMUNOASSAY
K926396 ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT
K931311 THYROID PEROXIDASE AUTO ANTIBODIES(TPO) IMMUN KIT
K930777 THYROGLOBULIN AUTOANTIBODY IMMUNOASSAY KIT
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