Abbot Aeroset Phenytoin Assay & Abbot Aeroset Phenytoin Calibrators

• • Terminated Z-2059-2008 FDA Unclassified (pre-2012) ·initiated 15 Feb 2008

  An Abbott investigation has determined that the phenytoin reagent does not maintain an onboard stability of 28 days as stated in the phenytoin package insert. In addition, the 14 day calibration interval is also not being met. Further investigation is required to determine the root cause of this issue. Until the cause has been determined and a corrective action defined, specific instructions ar

510(k) Number

K993026 ↗

FDA Product Code

DIP

Device Class

Class II

Regulation

21 CFR Part 862.3350

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

• C-Reactive Protein Control

  Class II

  FDA 510(k) K821412 Active Cleared 22 Jul 1982

• Ethyl Alcohol Serum Calibrator

  Class II

  FDA 510(k) K810466 Active Cleared 6 Mar 1981

• Micro Trak Xl System

  Class I

  FDA 510(k) K921747 Active Cleared 1 Oct 1992

• Syva Solid Phase Columns System II

  Class I

  FDA 510(k) K861392 Active Cleared 13 Jun 1986

• Modif. of Emit Cad Disopyramide Assay

  Class II

  FDA 510(k) K833623 Active Cleared 8 Dec 1983

• Emit Auto Cortisol Assay

  Class II

  FDA 510(k) K800245 Active Cleared 3 Mar 1980

See all devices from Syva Co. →