FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

EUROIMMUN ANTI-PLA2R IFA

K Number: DEN140002 · Decision May 29, 2014
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
1
Applicant Total
12
Review Days
62

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Basic Information

Device Name
EUROIMMUN ANTI-PLA2R IFA
K Number
DEN140002
Device Class
FDA class 2
Clearance Type
Post-NSE
Regulation Number
866.5780
Medical Specialty
Microbiology
Decision
Unknown
Applicant
Euroimmun US
Date Received
March 28, 2014
Decision Date
May 29, 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

K Number Device Name
K161513 Anti-Borrelia burgdorferi US Westernblot (IgG)
K142038 EUROIMMUN LYME ELISA(IgG/IgM)
K140224 EUROIMMUN EUROLINE ENA PROFILE 9AG (IGG)
K131791 IFA 40: HEP-20-10
K123660 25-OH VITAMIN D ELISA
K131185 ANA SCREEN ELISA (IGG)
K123261 EUROIMMUN ANTI-NRNP/SM ELISA (IGG)
K113439 EUROIMMUN EUROLINE PROFILE AUTOIMMUNE LIVER DISEASE 8AG (IGG)
K112996 EUROIMMUN ANTI-ENA POOL ELISA (IGG)
K112221 EUROIMMUN ANTI-SLA/LP ELISA(LGG)
Search all 12 clearances from Euroimmun US →