FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

Sofia Strep A+ FIA, Sofia 2 Analyzer

K Number: K171976 · Decision Dec 21, 2017
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
37
Review Days
174

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Basic Information

Device Name
Sofia Strep A+ FIA, Sofia 2 Analyzer
K Number
K171976
Device Class
FDA class 1
Clearance Type
Dual Track
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quidel Corporation
Date Received
June 30, 2017
Decision Date
December 21, 2017
Product Code
GTY
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
GTY Antigens, All Groups, Streptococcus Spp.

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