Nasal Cannula, with and Without Supply Tubing, and Other Similar Nasal Cannula Manufactured by Hrci

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

510(k) Number

K011125 ↗

FDA Product Code

CAT

Device Class

Class I

Regulation

21 CFR Part 868.5340

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Dual Lumen Oxygen Delivery Gas Sampling Cannula

  Class II

  FDA 510(k) K961150 Active Cleared 10 Sep 1996

• Conchatherm IV Heated Molecular Humidifier

  Class II

  FDA 510(k) K923946 Active Cleared 18 Oct 1994

• Smooth-Flo Circuit

  Class II

  FDA 510(k) K010402 Active Cleared 14 Mar 2001

• Model 780 Open recall

  Class II

  FDA 510(k) K031383 Active Cleared 7 Jul 2003

• Hudson Rci Lifesaver Single Patient Use Manual Resuscitator

  Class II

  FDA 510(k) K964719 Active Cleared 21 Feb 1997

• Side Draft Neb-U-Mist Nebulizer, Model 41896

  Class II

  FDA 510(k) K994352 Active Cleared 22 Mar 2000

See all devices from Hudson Respiratory Care, Inc. →