510(k) K053211

RDI HSFERRITIN KIT by Reference Diagnostics, Inc. — Product Code DBF

K053211 is an FDA 510(k) premarket notification submitted by Reference Diagnostics, Inc. for the device "RDI HSFERRITIN KIT". The FDA issued a decision of Substantially Equivalent on March 13, 2006. The device falls under product code DBF (Ferritin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5340. Reference Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 13, 2006
Date Received
November 16, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ferritin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5340
Review Panel
IM
Submission Type