510(k) K000469

RANDOX COMPLEMENT C3 by Randox Laboratories, Ltd. — Product Code CZW

K000469 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX COMPLEMENT C3". The FDA issued a decision of Substantially Equivalent on March 27, 2000. The device falls under product code CZW (Complement C3, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5240. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 27, 2000
Date Received
February 11, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Complement C3, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5240
Review Panel
IM
Submission Type