510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K141463Substantially Equivalent

Liason Xl1,25 Dihydroxyvitamin D; Control Set, Calibration Verifiers

Diasorin Inc., Stillwater MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141463 is the FDA 510(k) clearance record for LIASON XL1,25 DIHYDROXYVITAMIN D; CONTROL SET, CALIBRATION VERIFIERS, a class II device, cleared for DiaSorin, Inc. on under FDA product code MRG (System, Test, Vitamin D). FDA records list 74 510(k) clearances for DiaSorin, Inc., from to . As of , FDA records show no recalls naming K141463.

Clearance record

Decision date
Received
(190 days to decision)
Product code
MRG System, Test, Vitamin D
Regulation
21 CFR 862.1825
Device class
Class II
Review panel
Clinical Chemistry
Applicant
DiaSorin, Inc. 1951 Northwestern Ave., Stillwater MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRG

Trailing 12 months

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

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