510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K944202Substantially Equivalent

Abbott a-Gent Liquid Magnesium Reagent, Modified

Abbott Medical, Abbott Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K944202 is the FDA 510(k) clearance record for ABBOTT A-GENT LIQUID MAGNESIUM REAGENT, MODIFIED, a class I device, cleared for Abbott Laboratories on under FDA product code JGJ (Photometric Method, Magnesium). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K944202.

Clearance record

Decision date
Received
(95 days to decision)
Product code
JGJ Photometric Method, Magnesium
Regulation
21 CFR 862.1495
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Abbott Laboratories Dept: 09v8 Bldg: Ap5-2, Abbott Park IL
510(k) summary
Summary
Third party review
No

Clearances, product code JGJ

Trailing 12 months

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

FDA records show no clearances under product code JGJ in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JGJ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260