510(k) K002731

N LATEX B2-MICROGLOBULIN by Dade Behring, Inc. — Product Code JZG

K002731 is an FDA 510(k) premarket notification submitted by Dade Behring, Inc. for the device "N LATEX B2-MICROGLOBULIN". The FDA issued a decision of Substantially Equivalent on November 20, 2000. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Dade Behring, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 2000
Date Received
September 1, 2000
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