Gas Sampling Lines and Connectors Circuits

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K942124 ↗

FDA Product Code

CAI

Device Class

Class I

Regulation

21 CFR Part 868.5240

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• M.A.G. Inc. Ventilator Hoses

  Class I

  FDA 510(k) K942123 Active Cleared 22 Jun 1994

• M.A.G. Inc. Hyperinflation System

  Class I

  FDA 510(k) K942132 Active Cleared 22 Jun 1994

• M.A.G Inc. Adult Temperature Monitoring Anesthesia Circuits

  Class I

  FDA 510(k) K942129 Active Cleared 22 Jun 1994

• Pediatric Anesthesia Circuits

  Class I

  FDA 510(k) K942122 Active Cleared 22 Jun 1994

• Mag Connectors and Airway Extensions

  Class I

  FDA 510(k) K931800 Active Cleared 19 May 1993

• M.A.G. Inc. Guedel Airways

  Class I

  FDA 510(k) K942131 Active Cleared 22 Jun 1994

See all devices from Mag, Inc. →