510(k) K053126

BINAXNOW INFLUENZA A & B TEST by Binax, Inc. — Product Code PSZ

K053126 is an FDA 510(k) premarket notification submitted by Binax, Inc. for the device "BINAXNOW INFLUENZA A & B TEST". The FDA issued a decision of Substantially Equivalent on November 30, 2005. The device falls under product code PSZ (Devices Detecting Influenza A, B, And C Virus Antigens), a Class II device regulated under 21 CFR 866.3328. Binax, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 2005
Date Received
November 7, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Devices Detecting Influenza A, B, And C Virus Antigens
Device Class
Class II
Regulation Number
866.3328
Review Panel
MI
Submission Type

An influenza virus antigen detection test system is a device intended for the qualitative detection of influenza viral antigens directly from clinical specimens in patients with signs and symptoms of respiratory infection.