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

EUROIMMUN ANTI-DSDNA-NCX ELISA (IGG)

K Number: K083381 · Decision Apr 15, 2009
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
28
Applicant Total
19
Review Days
152

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Basic Information

Device Name
EUROIMMUN ANTI-DSDNA-NCX ELISA (IGG)
K Number
K083381
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
November 14, 2008
Decision Date
April 15, 2009
Product Code
LRM
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
LRM Anti-Dna Antibody (Enzyme-Labeled), 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)
K141827 EUROIMMUN IFA 40: HEP-20-10; EUROPATTERN MICROSCOPE AND SOFTWARE
K132195 EUROIMMUN ANTI-PLA2R ELISA (IGG)
Search all 19 clearances from Euroimmun Us, Inc. →