510(k) K980521

DIGOXIN ASSAY FOR THE TECHNICON RA / OPERA SYSTEMS by Bayer Corp. — Product Code KXT

K980521 is an FDA 510(k) premarket notification submitted by Bayer Corp. for the device "DIGOXIN ASSAY FOR THE TECHNICON RA / OPERA SYSTEMS". The FDA issued a decision of Substantially Equivalent on April 2, 1998. The device falls under product code KXT (Enzyme Immunoassay, Digoxin), a Class II device regulated under 21 CFR 862.3320. Bayer Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 2, 1998
Date Received
January 28, 1998
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