Medical Device
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K040241Substantially Equivalent

N-Geneous Wide Range Crp Reagent and Calibrator Set

Genzyme Corporation, Cambridge MA / Traditional, Substantially Equivalent

K040241 is the FDA 510(k) clearance record for N-GENEOUS WIDE RANGE CRP REAGENT AND CALIBRATOR SET, a class II device, cleared for Genzyme Corp. on under FDA product code DCK (C-Reactive Protein, Antigen, Antiserum, And Control). FDA records list 33 510(k) clearances for Genzyme Corp., from to . As of , FDA records show no recalls naming K040241.

Clearance record

Decision date
Received
(143 days to decision)
Product code
DCK C-Reactive Protein, Antigen, Antiserum, And Control
Regulation
21 CFR 866.5270
Device class
Class II
Review panel
Immunology
Applicant
Genzyme Corp. One Kendall Sq., Cambridge MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DCK

Trailing 12 months

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

FDA records show no clearances under product code DCK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DCK, 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