510(k) K033007

BAYER ADVIA DIGOXIN ASSAY FOR THE INTEGRATED MODULE SYSTEM by Bayer Diagnostics Corp. — Product Code KXT

K033007 is an FDA 510(k) premarket notification submitted by Bayer Diagnostics Corp. for the device "BAYER ADVIA DIGOXIN ASSAY FOR THE INTEGRATED MODULE SYSTEM". The FDA issued a decision of Substantially Equivalent on November 14, 2003. The device falls under product code KXT (Enzyme Immunoassay, Digoxin), a Class II device regulated under 21 CFR 862.3320. Bayer Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 2003
Date Received
September 26, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Digoxin
Device Class
Class II
Regulation Number
862.3320
Review Panel
TX
Submission Type