Arm-A-Care Nebulizer-Nebulizer

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

510(k) Number

K841990 ↗

FDA Product Code

CCQ

Device Class

Class I

Regulation

21 CFR Part 868.5640

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Arm-A-Care Humidifier-Respiratory Gas

  Class I

  FDA 510(k) K841991 Active Cleared 27 Jul 1984

• Arm-A-Vial Lv Sterial Water for Inhala

  Class I

  FDA 510(k) K841987 Active Cleared 27 Jul 1984

• Arm-A-Vial Lv Heater-Breathing Sys

  Class II

  FDA 510(k) K844005 Active Cleared 8 Nov 1984

• Arm-A-Vial Lv Sodium, Chloride Inhalat

  Class I

  FDA 510(k) K841988 Active Cleared 27 Jul 1984

• Arm-A-Flow Intravenous Flow Regulator

  Class II

  FDA 510(k) K842209 Active Cleared 4 Dec 1984

• Arm-A-Vial Lv Sodium Chloride Inhalat

  Class I

  FDA 510(k) K841989 Active Cleared 27 Jul 1984