Re-Trake Weiss Emergency Airway & Thoracic System

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

510(k) Number

K862909 ↗

FDA Product Code

BTO

FDA applicant

Intl. Medical Devices , Ltd.

Device Class

Class II

Regulation

21 CFR Part 868.5800

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Neo-Thor Thoracostomy Kit

  Class II

  FDA 510(k) K913541 Active Cleared 9 Apr 1992

• Pedia-Thor Thoracostomy Kit

  Class II

  FDA 510(k) K913540 Active Cleared 9 Apr 1992

• Respiration Monitor 1000

  Class II

  FDA 510(k) K820778 Active Cleared 3 May 1982

• Nu-Thor Thoracostomy Kit

  Class I

  FDA 510(k) K842666 Active Cleared 20 Sep 1984

• Thoracic Cathter Stylet

  Class I

  FDA 510(k) K913539 Active Cleared 21 Jan 1992

• Weiss Emergency Airway System

  Class II

  FDA 510(k) K790650 Active Cleared 27 Jun 1979

See all devices from Intl. Medical Devices, Ltd. →