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

IFA 40: HEP-20-10

K Number: K131791 · Decision Feb 26, 2014
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
12
Review Days
253

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Basic Information

Device Name
IFA 40: HEP-20-10
K Number
K131791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Euroimmun US
Date Received
June 18, 2013
Decision Date
February 26, 2014
Product Code
DHN
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
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

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