FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

UBI MAGIWEL(TM) HELICOBACTER PYLORI IGG

K Number: K924689 · Decision Aug 10, 1993
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
22
Review Days
327

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Basic Information

Device Name
UBI MAGIWEL(TM) HELICOBACTER PYLORI IGG
K Number
K924689
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
United Biotech, Inc.
Date Received
September 17, 1992
Decision Date
August 10, 1993
Product Code
LYR
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LYR Helicobacter Pylori

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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
K962211 UBI MAGIWEL THYROXINE (T4) QUANTITATIVE
K961236 UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE
K951993 UBI MAGIWEL FERRITIN QUANTITATIVE
K905473 UBI MAGIWEL CORTISOL QUANTITATIVE
Search all 22 clearances from United Biotech, Inc. →