510(k) K913024

ABBOTT QUICKSTART GAMMA-GLUTAMYTRANSFERASE TEST by Em Diagnostic Systems, Inc. — Product Code JQB

K913024 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "ABBOTT QUICKSTART GAMMA-GLUTAMYTRANSFERASE TEST". The FDA issued a decision of Substantially Equivalent on July 26, 1991. The device falls under product code JQB (Kinetic Method, Gamma-Glutamyl Transpeptidase), a Class I device regulated under 21 CFR 862.1360. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 26, 1991
Date Received
July 9, 1991
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