510(k) K002585

RANDOX TRANSFERRIN by Randox Laboratories, Ltd. — Product Code DDG

K002585 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX TRANSFERRIN". The FDA issued a decision of Substantially Equivalent on February 5, 2001. The device falls under product code DDG (Transferrin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5880. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 2001
Date Received
August 21, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Transferrin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5880
Review Panel
IM
Submission Type