510(k) K012112

RANDOX DIGITOXIN by Randox Laboratories, Ltd. — Product Code LFM

K012112 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX DIGITOXIN". The FDA issued a decision of Substantially Equivalent on January 11, 2002. The device falls under product code LFM (Enzyme Immunoassay, Digitoxin), a Class II device regulated under 21 CFR 862.3300. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 2002
Date Received
July 6, 2001
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