Oxygen/Pulse Monitor

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K875031 ↗

FDA Product Code

DQA

Device Class

Class II

Regulation

21 CFR Part 870.2700

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Healthdyne Impluse Ventilator

  Class II

  FDA 510(k) K853300 Active Cleared 15 Aug 1985

• Oxygen Concentrator, Model Bx-5000

  Class II

  FDA 510(k) K854374 Active Cleared 3 Jan 1986

• Healthdyne Event Recorder System

  Class II

  FDA 510(k) K860254 Active Cleared 30 Jan 1986

• Healthdyne Rate Meter

  Class II

  FDA 510(k) K874814 Active Cleared 11 Feb 1988

• Healthdyne's Apnea/Heart Monitor, Model 900S

  Class II

  FDA 510(k) K892006 Active Cleared 23 May 1989

• Ventilator, Infant Model 100

  Class II

  FDA 510(k) K781926 Active Cleared 21 Dec 1978

See all devices from Healthdyne, Inc. →