Inspiron Liquid Oxygen System

FDA 510(k) K834290 · Inspiron Corp.

Substantially Equivalent

510(k) numberK834290

Submission

Device name
Inspiron Liquid Oxygen System
Applicant
Inspiron Corp.
Walker, MI, US
Received
December 8, 1983
Decision date
February 4, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BYJ – Unit, Liquid-Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5655
Specialty
Anesthesiology

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K103324Precision Liquid Oxygen SystemBYJ · Traditional Precision Medical, Inc.04/21/2011SE
K101272Mass Oxygen Distribution System (Mods) Model 10C-0061-3BYJ · Traditional Essex Industries, Inc.08/20/2010SE
K081779GOLOX-93BYJ · Traditional Respironics, Inc.09/19/2008SE
K080023Modification to: SpiritBYJ · Special Caire, Inc.06/16/2008SE
K072723Respironics GoloxBYJ · Traditional Respironics, Inc.03/20/2008SE
K072011Copd Liquid Oxygen Portable, Model 300PBYJ · Traditional Copd Partners, Inc.10/18/2007SE
K071581Backpack Medical Oxygen SystemBYJ · Traditional Essex Cryogenics of Missouri, Inc.07/11/2007SE
K050153Spirit, Model HasBYJ · Traditional Caire, Inc.04/15/2005SE

More from Caire, Inc.

510(k)DeviceDecision
K860838Inspiron Double Swivel Trach AdapterBZA · Traditional 04/09/1986SE
K850346Oxygen ConcentratorCAW · Traditional 02/04/1985SE
K843932Vapor-Phase Humidifier Sys-AdvancedBTT · Traditional 10/18/1984SE
K840935Manual Resuscitation SystemBTM · Traditional 04/05/1984SE
K841158Nebulo 28 Nebulizer KitBTT · Traditional 03/30/1984SE
K840418Inspiratory/Expiratory Muscle ExercisBWF · Traditional 02/17/1984SE
K772072Manifold & Nebu. for Doub. Line Mach.CAF · Traditional 11/15/1977SE
K772071Manifold & Nebu. for Single Line Mach.CAF · Traditional 11/15/1977SE
K772070Ventilator Setup, VolumeCAF · Traditional 11/15/1977SE
K772069Vol. Ventilator Setup W/Out NebulizerBZO · Traditional 11/15/1977SE

Questions and answers

When was Inspiron Liquid Oxygen System cleared by the FDA?

Inspiron Liquid Oxygen System (K834290) received a 510(k) decision of Substantially Equivalent on February 4, 1984, 58 days after the submission was received.

What is the product code of K834290?

The FDA product code is BYJ – Unit, Liquid-Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5655.