510(k) K033234

IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZER by Diagnostic Products Corp. — Product Code DHA

K033234 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZER". The FDA issued a decision of Substantially Equivalent on December 12, 2003. The device falls under product code DHA (System, Test, Human Chorionic Gonadotropin), a Class II device regulated under 21 CFR 862.1155. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 12, 2003
Date Received
October 6, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Human Chorionic Gonadotropin
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type