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

UBI MAGIWEL CORTISOL QUANTITATIVE

K Number: K905473 · Decision Jan 31, 1991
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
83
Applicant Total
22
Review Days
56

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Basic Information

Device Name
UBI MAGIWEL CORTISOL QUANTITATIVE
K Number
K905473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1205
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
United Biotech, Inc.
Date Received
December 6, 1990
Decision Date
January 31, 1991
Product Code
CGR
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
CGR Radioimmunoassay, Cortisol

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Other Clearances by United Biotech, Inc.

K Number Device Name
K981573 UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVE
K973154 UBI MAGIWEL MARIJUANA METABOLITES
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
K924689 UBI MAGIWEL(TM) HELICOBACTER PYLORI IGG
Search all 22 clearances from United Biotech, Inc. →