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

SIMPLEXA FLU A/B & RSV

K Number: K102170 · Decision Nov 24, 2010
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
14
Review Days
114

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Basic Information

Device Name
SIMPLEXA FLU A/B & RSV
K Number
K102170
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Focus Diagnostics, Inc.
Date Received
August 2, 2010
Decision Date
November 24, 2010
Product Code
OCC
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
OCC Respiratory Virus Panel Nucleic Acid Assay System

Similar 510(k) Clearances

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

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Other Clearances by Focus Diagnostics, Inc.

K Number Device Name
K152408 Simplexa Flu A/B & RSV Direct and Simplexa Flu A/B & RSV Positive Control Pack
K143651 Simplexa Group A Strep Direct, Simplexa Group A Strep Positive Control Pack
K120986 STRATIFY JCV DXSELECT
K120413 SIMPLEXA FLU A/B & RSV DIRECT, SIMPLEXA FLU A/B & RSV POSITIVE CONTROL PACK
K113433 SIMPLEXA C. DIFFICILE UNIVERSAL DIRECT
DEN120008 STRATIFY JCV(TM) ANTIBODY
K102314 3M INTEGRATED CYCLER (110V) & (220V)
K100148 SIMPLEXA INFLUENZA A H1N1 (2009) MODEL MOL2500
K073381 PLEXUS EBV IGM MULTI-ANALYTE DIAGNOSTICS, MODEL: MP0600M
K073382 PLEXUS EBV IGG MULTI-ANALYTE DIAGNOSTICS, MODEL: MP0500G
Search all 14 clearances from Focus Diagnostics, Inc. →