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

Alere i Influenza A & B 2, Alere i Instrument, Alere i Influenza A & B Control Swab Kit

K Number: K171792 · Decision Sep 29, 2017
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
78
Applicant Total
17
Review Days
105

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Basic Information

Device Name
Alere i Influenza A & B 2, Alere i Instrument, Alere i Influenza A & B Control Swab Kit
K Number
K171792
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3980
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alere Scarborough, Inc.
Date Received
June 16, 2017
Decision Date
September 29, 2017
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 Alere Scarborough, Inc.

K Number Device Name
DEN180014 WOUNDCHEK Bacterial Status
K190204 ID NOW Influenza A & B 2
K181853 Alere BinaxNOW Influenza A & B Card 2, Alere Reader
K173653 Alere i Strep A 2, Alere i instrument, Alere i Strep A 2 Control Swab Kit
K173932 Alere i Influenza A & B, Alere i Strep A, Alere i RSV, Alere i Influenza A & B 2
K173502 Alere BinaxNOW Influenza A & B Card 2, Alere Reader, Alere BinaxNOW Influenza A & B Card 2 Control Swab Kit
K162642 Alere BinaxNOW Influenza A & B Card 2, Alere Reader, Alere BinaxNOW Influenza A & B Card 2 Control Swab Kit
K163266 Alere i Influenza A & B, Alere i Influenza A & B Control Swab Kit, Alere i Instrument
K161375 Alere i RSV, Alere i Instrument, Alere i RSV Control Swab Kit
K161364 BinaxNOW G6PD Test
Search all 17 clearances from Alere Scarborough, Inc. →