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

QUICK VUE RSV TEST, MODELS 20193, 20199

K Number: K070747 · Decision Apr 23, 2007
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
30
Applicant Total
93
Review Days
35

Basic Information

Device Name
QUICK VUE RSV TEST, MODELS 20193, 20199
K Number
K070747
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3480
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
QUIDEL CORP.
Date Received
March 19, 2007
Decision Date
April 23, 2007
Product Code
GQG
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
GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

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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
K123998 QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY
K122189 QUIDEL MOLECULAR RSV + HMPV ASSAY
K113777 QUIDEL MOLECULAR INFLUENZA A+B
K112172 QUIDEL MOLECULAR INFLUENZA A + B ASSAY
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