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

GROUP A STREP POSITIVE AND NEGATIVE CONTROLS

K Number: K912868 · Decision Aug 7, 1991
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
93
Review Days
40

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Basic Information

Device Name
GROUP A STREP POSITIVE AND NEGATIVE CONTROLS
K Number
K912868
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quidel Corp.
Date Received
June 28, 1991
Decision Date
August 7, 1991
Product Code
GTZ
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
GTZ Antisera, All Groups, Streptococcus Spp.

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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
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