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

TOTAL T3 CHEMILUMINESCENCE ASSAY

K Number: K923015 · Decision Sep 2, 1992
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
68
Review Days
72

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Basic Information

Device Name
TOTAL T3 CHEMILUMINESCENCE ASSAY
K Number
K923015
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nichols Institute Diagnostics
Date Received
June 22, 1992
Decision Date
September 2, 1992
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 Diagnostics

K Number Device Name
K050784 NICHOLS ADVANTAGE ALDOSTERONE ASSAY
K042676 NICHOLS ADVANTAGE HYPERGLYCOSYLATED HUMAN CHORIONIC GONADOTROPIN (H-HCG) ASSAY
K042689 NICHOLS ADVANTAGE CORTISOL
K040813 NICHOLS ADVANTAGE CHEMILUMINESCENCE INTACT PARATHYROID HORMONE, MODEL 62-7022
K033727 NICHOLS ADVANTAGE BIO-INTACT PTH (1-84) IMMUNOASSAY
K033302 NICHOLS ADVANTAGE BIO-INTACT PTH (1-84) ASSAY, MODEL 62-7040
K032188 NICHOLS ADVANTAGE ALDOSTERONE ASSAY
K022356 NICHOLS ADVANTAGE CHEMILUMINESCENCE HELICOBACTOR PYLORI IGG ANTIBODIES IMMUNOASSAY
K022472 PARATHYROID HORMONE TEST SYSTEM/NICHOLS ADVANTAGE QUICK-INTRAOPERATIVE BIO-INTACT PTH (1-84)
K013992 NICHOLS ADVANTAGE CHEMILUMINESCENCE BIO-INTACT PARATHYROID HORMONE (1-84) IMMUNOASSAY
Search all 68 clearances from Nichols Institute Diagnostics →