Agilent Component Monitoring System, Agilent Cardiac Output Module, Agilent Invasive Pressure Module, Model M1175A/76A

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

510(k) Number

K002758 ↗

FDA Product Code

DSI

Device Class

Class II

Regulation

21 CFR Part 870.1025

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Agilent Component Monitoring System, Agilent Multi-Measurement Server and Compact Portable Patient Monitor, Agilent Noni

  Class II

  FDA 510(k) K001333 Active Cleared 17 May 2000

• Agilent Component Monitoring System; Agilent Invasive Blood Pressure Module

  Class II

  FDA 510(k) K001722 Active Cleared 30 Jun 2000

• Agilent Component Monitoring System, Agilent V24/26, Agilent Bis Module, Model M1175A/76A/77A, Rev.l, M1205A, Rev.l, M1034A

  Class II

  FDA 510(k) K003038 Active Cleared 15 Dec 2000