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

EUROIMMUN ANTI-PLA2R ELISA (IGG)

K Number: K132195 · Decision Jun 27, 2014
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
1
Applicant Total
19
Review Days
347

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Basic Information

Device Name
EUROIMMUN ANTI-PLA2R ELISA (IGG)
K Number
K132195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Euroimmun Us, Inc.
Date Received
July 15, 2013
Decision Date
June 27, 2014
Product Code
PGV
Advisory Committee
Microbiology
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
PGV Anti-Phospholipase A2 Receptor

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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
K100017 EUROIMMUN HIPPOCAMPUS/CEREBELLUM/GLUTAMATE RECEPTOR/IFA BIOCHIP MOSAIC TEST SYSTEM
Search all 19 clearances from Euroimmun Us, Inc. →