510(k) K935554

QUIKPAC II ONESTEP STREP A IMMUNOCHROMATOGRAPHIC ASSAY by Syntron Bioresearch, Inc. — Product Code GTZ

K935554 is an FDA 510(k) premarket notification submitted by Syntron Bioresearch, Inc. for the device "QUIKPAC II ONESTEP STREP A IMMUNOCHROMATOGRAPHIC ASSAY". The FDA issued a decision of Substantially Equivalent on August 30, 1995. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Syntron Bioresearch, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1995
Date Received
November 17, 1993
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