Regulator Oxygen Mechanical

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K863711 ↗

FDA Product Code

CAN

Device Class

Class I

Regulation

21 CFR Part 868.2700

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Monopolar Electrode

  Class II

  FDA 510(k) K915296 Active Cleared 3 Sep 1992

• Single Use Manual Resuscitator

  Class II

  FDA 510(k) K881087 Active Cleared 14 Apr 1988

• Levy Articulating Retractor

  Class I

  FDA 510(k) K920471 Active Cleared 23 Jun 1992

• Lifeguard Gas Sampling Line for Mass Spectrometry

  Class I

  FDA 510(k) K880959 Active Cleared 14 Apr 1988

• Regulator Flowmeter

  Class I

  FDA 510(k) K915505 Active Cleared 22 Apr 1992

• Lifeguard Bacterial and Viral Filter

  Class II

  FDA 510(k) K880958 Active Cleared 27 Apr 1988

See all devices from Lifeguard Medical Products, Inc. →