510(k) K012521

BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST by Binax, Inc. — Product Code GTZ

K012521 is an FDA 510(k) premarket notification submitted by Binax, Inc. for the device "BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST". The FDA issued a decision of Substantially Equivalent on November 30, 2001. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Binax, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 2001
Date Received
August 6, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, All Groups, Streptococcus Spp.
Device Class
Class I
Regulation Number
866.3740
Review Panel
MI
Submission Type