510(k) K072078

QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307 by Biokit, S.A. — Product Code JZG

K072078 is an FDA 510(k) premarket notification submitted by Biokit, S.A. for the device "QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307". The FDA issued a decision of Substantially Equivalent on December 19, 2007. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Biokit, S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 19, 2007
Date Received
July 30, 2007
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