Marquest Sct 2000, Heated Humidification System

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

510(k) Number

K880979 ↗

FDA Product Code

BTT

Device Class

Class II

Regulation

21 CFR Part 868.5450

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Circuit Breathing

  Class I

  FDA 510(k) K840740 Active Cleared 17 Apr 1984

• Dispos. Anesthesia Face Mask

  Class I

  FDA 510(k) K840535 Active Cleared 21 Feb 1984

• Disposable Non-Rebreathing Anes. Circuit

  Class I

  FDA 510(k) K823714 Active Cleared 7 Jan 1983

• C-CO2 Colorimetric CO2 Indicator

  Class II

  FDA 510(k) K050066 Active Cleared 1 Mar 2005

• Disposable Anesthesia Breathing Circuit

  Class I

  FDA 510(k) K822379 Active Cleared 20 Aug 1982

• Temp Marq Convective Warming System

  Class II

  FDA 510(k) K904690 Active Cleared 1 Feb 1991

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