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

EUROIMMUN HIPPOCAMPUS/CEREBELLUM/GLUTAMATE RECEPTOR/IFA BIOCHIP MOSAIC TEST SYSTEM

K Number: K100017 · Decision Sep 13, 2010
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
0
Applicant Total
19
Review Days
252

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Basic Information

Device Name
EUROIMMUN HIPPOCAMPUS/CEREBELLUM/GLUTAMATE RECEPTOR/IFA BIOCHIP MOSAIC TEST SYSTEM
K Number
K100017
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Euroimmun Us, Inc.
Date Received
January 4, 2010
Decision Date
September 13, 2010
Product Code
OSK
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
OSK Anti-Glutamate Receptor (Type Nmda) Ifa

Other Clearances by Euroimmun Us, Inc.

K Number Device Name
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K172252 EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern
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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. →