Mrm-2 Oxygen Consumption Monitor

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K801852 ↗

FDA Product Code

BZL

Device Class

Class II

Regulation

21 CFR Part 868.1730

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Cardiac Computers, Co-10 & Co-10R

  Class II

  FDA 510(k) K781805 Active Cleared 29 Jan 1979

• 7FRENCH Flow Directed Triple Lumen Cath

  Class II

  FDA 510(k) K802481 Active Cleared 31 Oct 1980

• Pab Convenience Tray

  Class I

  FDA 510(k) K781264 Active Cleared 20 Sep 1978

• 4F Sterile Balloon-Less, Catheter 913-28

  Class II

  FDA 510(k) K791026 Active Cleared 22 Jun 1979

• System Controller 720 Series

  Class I

  FDA 510(k) K791661 Active Cleared 24 Sep 1979

• Calibrator, Dynamic

  Class II

  FDA 510(k) K781692 Active Cleared 29 Nov 1978

See all devices from Waters Assoc., Inc. →