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

QUICKVUE INFLUENZA A + B TEST

K Number: K053146 · Decision Dec 14, 2005
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
71
Applicant Total
93
Review Days
34

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Basic Information

Device Name
QUICKVUE INFLUENZA A + B TEST
K Number
K053146
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3328
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quidel Corp.
Date Received
November 10, 2005
Decision Date
December 14, 2005
Product Code
PSZ
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
PSZ Devices Detecting Influenza A, B, And C Virus Antigens

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PSZ), ordered by most recent decision date.

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Other Clearances by Quidel Corp.

K Number Device Name
K131813 QUIDEL MOLECULAR RSV + HMPV ASSAY
K131728 QUIDEL MOLECULAR INFLUENZA A + B ASSAY
K130398 SOFIA(R) RSV FIA
K131166 SOFIA(R) HCG FIA
K131606 SOFIA INFLUENZA A+B FIA
K131619 QUICKVUE INFLUENZA A+B
K122189 QUIDEL MOLECULAR RSV + HMPV ASSAY
K123998 QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY
K113777 QUIDEL MOLECULAR INFLUENZA A+B
K112172 QUIDEL MOLECULAR INFLUENZA A + B ASSAY
Search all 93 clearances from Quidel Corp. →