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Alere i Influenza A & B, Alere i Strep A, Alere i RSV, Alere i Influenza A & B 2

K173932 Class II Special
Decision Date
2018-01-26
Sponsor / Applicant
Alere Scarborough, Inc.

Technical Specification

510(k) Submission ID K173932
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2018-01-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Alere i Influenza A & B, Alere i Strep A, Alere i RSV, Alere i Influenza A & B 2 received FDA 510(k) clearance under submission number K173932, sponsored by Alere Scarborough, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2018-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code OCC and 21 CFR 866.3980, within the Microbiology review panel as a Class II device.