510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142346Substantially Equivalent

Urine/CSF Albumin, Urine/CSF Albumin Calibrator

Beckman Coulter Ireland Inc, Co. Clare, IE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142346 is the FDA 510(k) clearance record for Urine/CSF Albumin, Urine/CSF Albumin Calibrator, a class II device, cleared for Beckman Coulter Ireland, Inc. on under FDA product code DCF (Albumin, Antigen, Antiserum, Control). FDA records list 7 510(k) clearances for Beckman Coulter Ireland, Inc., from to . As of , FDA records show no recalls naming K142346.

Clearance record

Decision date
Received
(54 days to decision)
Product code
DCF Albumin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5040
Device class
Class II
Review panel
Immunology
Applicant
Beckman Coulter Ireland, Inc. Lismeehan, Co. Clare, IE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DCF

Trailing 12 months

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

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