510(k) K931958

SYNERMED GGT REAGENT KIT by Synermed, Inc. — Product Code JQB

K931958 is an FDA 510(k) premarket notification submitted by Synermed, Inc. for the device "SYNERMED GGT REAGENT KIT". The FDA issued a decision of Substantially Equivalent on September 8, 1993. The device falls under product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase), a Class I device regulated under 21 CFR 862.1360. Synermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 1993
Date Received
April 20, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kinetic Method, Gamma-Glutamyl Transpeptidase
Device Class
Class I
Regulation Number
862.1360
Review Panel
CH
Submission Type