510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000469Substantially Equivalent

Randox Complement C3

Randox Laboratories, Limited, Crumlin, IE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000469 is the FDA 510(k) clearance record for RANDOX COMPLEMENT C3, a class II device, cleared for Randox Laboratories, Ltd. on under FDA product code CZW (Complement C3, Antigen, Antiserum, Control). FDA records list 134 510(k) clearances for Randox Laboratories, Ltd., from to . As of , FDA records show no recalls naming K000469.

Clearance record

Decision date
Received
(45 days to decision)
Product code
CZW Complement C3, Antigen, Antiserum, Control
Regulation
21 CFR 866.5240
Device class
Class II
Review panel
Immunology
Applicant
Randox Laboratories, Ltd. Ardmore, Diamond Rd., Crumlin, IE
510(k) summary
Summary
Third party review
No

Clearances, product code CZW

Trailing 12 months

FDA records hold no clearances under product code CZW in the trailing twelve months.

FDA records show no clearances under product code CZW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CZW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260