Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K981581Substantially Equivalent

Iron

Abbott Medical, Irving TX / Traditional, Substantially Equivalent

K981581 is the FDA 510(k) clearance record for IRON, a class I device, cleared for Abbott Laboratories on under FDA product code CFM (Bathophenanthroline, Colorimetry, Iron (Non-Heme)). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K981581.

Clearance record

Decision date
Received
(35 days to decision)
Product code
CFM Bathophenanthroline, Colorimetry, Iron (Non-Heme)
Regulation
21 CFR 862.1410
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories Dept. 09va Lc-2, Irving TX
510(k) summary
Summary
Third party review
No

Clearances, product code CFM

Trailing 12 months

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

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