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

Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex)

K Number: K143653 · Decision Sep 4, 2015
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
16
Review Days
255

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Basic Information

Device Name
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex)
K Number
K143653
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nanosphere, Inc.
Date Received
December 23, 2014
Decision Date
September 4, 2015
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 Nanosphere, Inc.

K Number Device Name
K140083 VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST ( EP)
K132843 VERIGENE GRAM NEGATIVE BLOOD CULTURE NUCLEIC ACID TEST (BC-GN)
K123197 VERIGENE C. DIFFICILE NUCLEIC ACID TEST (CDF)
K120466 VERIGENE CYP2C19 NUCLEIC ACID TES (2C19)
K122514 VERIGENE GRAM-POSITIVE BLOOD CULTURE (GC-GP) NUCLEIC ACID TEST
DEN120014 VERIGENE GRAM POSITIVE BLOOD CULTURE NUCLEIC ACID TEST (BC-GP)
K112424 VERIGENE STAPHYLOCOCCUS BLOOD CULTURE NUCLEIC ACID TEST (BC-S)
K103209 VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST +(RVNAT+)
K093337 VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST ON THE VERIGENE SP SYSTEM
K092957 VERIGENE SYSTEM, VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST
Search all 16 clearances from Nanosphere, Inc. →