510(k) K970546

ACS DIGITOXIN by Chiron Diagnostics Corp. — Product Code LFM

K970546 is an FDA 510(k) premarket notification submitted by Chiron Diagnostics Corp. for the device "ACS DIGITOXIN". The FDA issued a decision of Substantially Equivalent on July 14, 1997. The device falls under product code LFM (Enzyme Immunoassay, Digitoxin), a Class II device regulated under 21 CFR 862.3300. Chiron Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1997
Date Received
February 12, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Digitoxin
Device Class
Class II
Regulation Number
862.3300
Review Panel
TX
Submission Type