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

UBI MAGIWEL THYROXINE (T4) QUANTITATIVE

K Number: K962211 · Decision Jul 8, 1996
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
85
Applicant Total
22
Review Days
28

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Basic Information

Device Name
UBI MAGIWEL THYROXINE (T4) QUANTITATIVE
K Number
K962211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1700
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
United Biotech, Inc.
Date Received
June 10, 1996
Decision Date
July 8, 1996
Product Code
KLI
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
KLI Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine

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K Number Device Name
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K973692 UBI MAGIWEL C-REACTIVE PROTEIN(CRP) QUANTITATIVE
K973153 UBI MAGIWEL AMPHETAMINE METABOLITES
K973156 UBI MAGIWEL COCAINE METABOLITES
K973155 UBI MAGIWEL OPIATE METABOLITES
K961236 UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE
K951993 UBI MAGIWEL FERRITIN QUANTITATIVE
K924689 UBI MAGIWEL(TM) HELICOBACTER PYLORI IGG
K905473 UBI MAGIWEL CORTISOL QUANTITATIVE
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