510(k) K063045

IMMULITE 2000, IMMULITE 2500 VANCOMYCIN by Diagnostic Products Corp. — Product Code LEH

K063045 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE 2000, IMMULITE 2500 VANCOMYCIN". The FDA issued a decision of Substantially Equivalent on December 5, 2006. The device falls under product code LEH (Radioimmunoassay, Vancomycin), a Class II device regulated under 21 CFR 862.3950. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 2006
Date Received
October 4, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Vancomycin
Device Class
Class II
Regulation Number
862.3950
Review Panel
TX
Submission Type