510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K060423Substantially Equivalent

Cyan Dxd, Multitest Cd8/cd4/cd3, Cd3-Fitc, Cd3-Rpe, Cd3-Apc and Fluorospheres

Agilent Technologies, Inc., Carpinteria CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060423 is the FDA 510(k) clearance record for CYAN DXD, MULTITEST CD8/CD4/CD3, CD3-FITC, CD3-RPE, CD3-APC AND FLUOROSPHERES, a class II device, cleared for Dakocytomation California, Inc. on under FDA product code GKZ (Counter, Differential Cell). FDA records list 51 510(k) clearances for Agilent Technologies, Inc., from to . As of , FDA records show no recalls naming K060423.

Clearance record

Decision date
Received
(179 days to decision)
Product code
GKZ Counter, Differential Cell
Regulation
21 CFR 864.5220
Device class
Class II
Review panel
Hematology
Applicant
Dakocytomation California, Inc. 6392 Via Real, Carpinteria CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GKZ

Trailing 12 months
4 clearances under product code GKZ in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GKZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260