Manifold & Nebulizer, Universal

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K772068 ↗

FDA Product Code

CAF

Device Class

Class II

Regulation

21 CFR Part 868.5630

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Manifold & Nebu. for Single Line Mach.

  Class II

  FDA 510(k) K772071 Active Cleared 15 Nov 1977

• Pediatric Anesthesia Circuit

  Class I

  FDA 510(k) K770549 Active Cleared 30 Mar 1977

• Filter, Bacteria (#2290)

  Class II

  FDA 510(k) K760081 Active Cleared 15 Jul 1976

• Inspiron Liquid Oxygen System

  Class II

  FDA 510(k) K834290 Active Cleared 4 Feb 1984

• Cannula, Nasal, for Oxygen

  Class I

  FDA 510(k) K760080 Active Cleared 15 Jul 1976

• Vapor-Phase Humidifier Sys-Advanced

  Class II

  FDA 510(k) K843932 Active Cleared 18 Oct 1984

See all devices from Inspiron Corp. →