510(k) K943235

IMMULITE DIGITOXIN by Diagnostic Products Corp. — Product Code LFM

K943235 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE DIGITOXIN". The FDA issued a decision of Substantially Equivalent on October 27, 1994. The device falls under product code LFM (Enzyme Immunoassay, Digitoxin), a Class II device regulated under 21 CFR 862.3300. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1994
Date Received
July 6, 1994
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