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

COTUBE ESTRADIOL RADIOIMMUNOASSAY

K Number: K931740 · Decision Aug 16, 1993
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
49
Applicant Total
319
Review Days
131

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Basic Information

Device Name
COTUBE ESTRADIOL RADIOIMMUNOASSAY
K Number
K931740
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Rad
Date Received
April 7, 1993
Decision Date
August 16, 1993
Product Code
CHP
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
CHP Radioimmunoassay, Estradiol

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