510(k) K011709

UNI-GOLD STREP A TEST KIT by Trinity Biotech, Plc — Product Code GTZ

K011709 is an FDA 510(k) premarket notification submitted by Trinity Biotech, Plc for the device "UNI-GOLD STREP A TEST KIT". The FDA issued a decision of Substantially Equivalent on November 8, 2001. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Trinity Biotech, Plc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 2001
Date Received
June 4, 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