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

Sofia 2 Campylobacter FIA

K Number: K211342 · Decision Nov 23, 2021
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
11
Applicant Total
37
Review Days
204

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Basic Information

Device Name
Sofia 2 Campylobacter FIA
K Number
K211342
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quidel Corporation
Date Received
May 3, 2021
Decision Date
November 23, 2021
Product Code
LQP
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
LQP Campylobacter Spp.

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K230236 Lyra Influenza A+B Assay
K173496 Sofia 2 Lyme FIA, Sofia Lyme Control Set
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K173691 Sofia Lyme FIA, Sofia 2 analyzer, Sofia 2 Installation Pack
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