510(k) K935181

ASPARTATE AMINOTRANSFERASE (AST) TEST by Em Diagnostic Systems, Inc. — Product Code CIT

K935181 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "ASPARTATE AMINOTRANSFERASE (AST) TEST". The FDA issued a decision of Substantially Equivalent on January 27, 1994. The device falls under product code CIT (Nadh Oxidation/Nad Reduction, Ast/Sgot), a Class II device regulated under 21 CFR 862.1100. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1994
Date Received
October 26, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nadh Oxidation/Nad Reduction, Ast/Sgot
Device Class
Class II
Regulation Number
862.1100
Review Panel
CH
Submission Type