510(k) K032692

DAKOCYTOMATION BETA-2-MICROGLOBULIN KIT, CODE NO. OA 368 by Dako A/S — Product Code JZG

K032692 is an FDA 510(k) premarket notification submitted by Dako A/S for the device "DAKOCYTOMATION BETA-2-MICROGLOBULIN KIT, CODE NO. OA 368". The FDA issued a decision of Substantially Equivalent on January 22, 2004. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Dako A/S has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 2004
Date Received
September 2, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Beta-2-Microglobulin Immunological
Device Class
Class II
Regulation Number
866.5630
Review Panel
IM
Submission Type