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

Anti-Borrelia burgdorferi US Westernblot (IgG)

K Number: K161513 · Decision Aug 25, 2016
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
109
Applicant Total
12
Review Days
84

Basic Information

Device Name
Anti-Borrelia burgdorferi US Westernblot (IgG)
K Number
K161513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
EUROIMMUN US
Date Received
June 2, 2016
Decision Date
August 25, 2016
Product Code
LSR
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LSR Reagent, Borrelia Serological Reagent

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