King Diagnostics Magnesium Reagent

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K923927 ↗

FDA Product Code

JGJ

Device Class

Class I

Regulation

21 CFR Part 862.1495

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• King Diagnostics Phosphorus Test

  Class I

  FDA 510(k) K811749 Active Cleared 10 Jul 1981

• Potassium Test

  Class II

  FDA 510(k) K811661 Active Cleared 25 Jun 1981

• Acid Phosphatase Test

  Class II

  FDA 510(k) K873726 Active Cleared 27 Jan 1988

• Calibration Kit

  Class II

  FDA 510(k) K882220 Active Cleared 2 Aug 1988

• King Diagnostics Ldh Test

  Class II

  FDA 510(k) K862306 Active Cleared 19 Aug 1986

• Albumin Test

  Class II

  FDA 510(k) K811662 Active Cleared 25 Jun 1981

See all devices from King Diagnostics, Inc. →