510(k) K922947

GAMMA GULTAMYL TRANSFERASE TEST by Em Diagnostic Systems, Inc. — Product Code JQB

K922947 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "GAMMA GULTAMYL TRANSFERASE TEST". The FDA issued a decision of Substantially Equivalent on September 28, 1992. 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
September 28, 1992
Date Received
June 18, 1992
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