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

UBI MAGIWEL(TM) PROLACTIN QUANTATIVE

K Number: K864075 · Decision Dec 16, 1986
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
79
Applicant Total
22
Review Days
57

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Basic Information

Device Name
UBI MAGIWEL(TM) PROLACTIN QUANTATIVE
K Number
K864075
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
United Biotech, Inc.
Date Received
October 20, 1986
Decision Date
December 16, 1986
Product Code
CFT
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
CFT Radioimmunoassay, Prolactin (Lactogen)

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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. →