Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K153375Substantially Equivalent

ARCHITECT 25-OH Vitamin D 5P02, ARCHITECT 25-OH Vitamin D 5P02 Calibrators, ARCHITECT 25-OH Vitamin D 5P02 Controls

Abbott Medical, Abbott Park IL / Traditional, Substantially Equivalent

K153375 is the FDA 510(k) clearance record for ARCHITECT 25-OH Vitamin D 5P02, ARCHITECT 25-OH Vitamin D 5P02 Calibrators, ARCHITECT 25-OH Vitamin D 5P02 Controls, a class II device, cleared for Abbott Laboratories on under FDA product code MRG (System, Test, Vitamin D). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show one recall naming K153375.

Clearance record

Decision date
Received
(263 days to decision)
Product code
MRG System, Test, Vitamin D
Regulation
21 CFR 862.1825
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories Dept 093e, Bldg. Ap 8, 100 Abbott Park Rd., Abbott Park IL
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