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

EUROIMMUN IFA 40: HEP-20-10; EUROPATTERN MICROSCOPE AND SOFTWARE

K Number: K141827 · Decision Apr 17, 2015
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
19
Review Days
284

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Basic Information

Device Name
EUROIMMUN IFA 40: HEP-20-10; EUROPATTERN MICROSCOPE AND SOFTWARE
K Number
K141827
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Euroimmun Us, Inc.
Date Received
July 7, 2014
Decision Date
April 17, 2015
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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Other Clearances by Euroimmun Us, Inc.

K Number Device Name
K193115 EUROIMMUN Anti-BP230-CF ELISA (IgG)
K183313 EUROIMMUN Anti-tissue Transglutaminase ELISA (IgA), EUROIMMUN Anti-tissue Transglutaminase ELISA (IgG)
K172582 EUROIMMUN IFA Granulocyte Mosaic™ EUROPattern and EUROIMMUN EUROPLUS Granulocyte Mosaic™ EUROPattern
K172244 EUROIMMUN IFA: Crithidia luciliae (anti-dsDNA) EUROPattern
K172252 EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern
K172722 Anti-Borrelia burgdorferi US EUROLINE-WB (IgM)
K153308 EUROIMMUN Anti-West Nile Virus ELISA (IgM)
K153303 EUROIMMUN Anti-West Nile Virus ELISA (IgG)
K132195 EUROIMMUN ANTI-PLA2R ELISA (IGG)
K100017 EUROIMMUN HIPPOCAMPUS/CEREBELLUM/GLUTAMATE RECEPTOR/IFA BIOCHIP MOSAIC TEST SYSTEM
Search all 19 clearances from Euroimmun Us, Inc. →