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

UBI MAGIWEL(TM) ANA QUANTITATIVE

K Number: K910033 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
111
Applicant Total
22
Review Days
21

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Basic Information

Device Name
UBI MAGIWEL(TM) ANA QUANTITATIVE
K Number
K910033
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
United Biotech, Inc.
Date Received
January 4, 1991
Decision Date
January 25, 1991
Product Code
LJM
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

Similar 510(k) Clearances

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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. →