510(k) K960712

BINAX STREP A TEST by Binax, Inc. — Product Code GTZ

K960712 is an FDA 510(k) premarket notification submitted by Binax, Inc. for the device "BINAX STREP A TEST". The FDA issued a decision of Substantially Equivalent on March 22, 1996. 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
March 22, 1996
Date Received
February 21, 1996
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