Antistatic Compact Space Chamber

FDA 510(k) K143615 · Medical Developments International Limited

Substantially Equivalent

510(k) numberK143615

Submission

Device name
Antistatic Compact Space Chamber
Applicant
Medical Developments International Limited
Springvale, AU
Received
December 19, 2014
Decision date
January 26, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
NVP – Holding Chambers, Direct Patient Interface
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

Holding chambers are devices that are used with nebulizers and metered dose inhalers and are comprised of a reservoir into which an aerosol medication is dispensed. A holding chamber uses a valved mouthpiece through which the patient inhales the dispensed medication. Holding chambers are intended to minimize delivery of large aerosolized particles

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K160109Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding ChamberNVP · Traditional Thayer Medical Corporation05/19/2017SE
K140062FSC Anti-Static Valved Collapsible Holding ChamberNVP · Traditional Fsc Laboratories, Inc.10/03/2014SE
K122252Space Chamber Plus Compact Space Chamber PlusNVP · Traditional Medical Developments International11/13/2013SE
K130598Inspirachamber Anti-Static Valved Holding ChamberNVP · Traditional Inspirx, Inc.06/05/2013SE
K112010Aerochamber Plus Flow-Vu Anti-Static Valved Holding Chamber (VHC)NVP · Traditional Trudell Medical Intl.07/11/2012SE
K110293Optichamber Diamond Valved Holding ChamberNVP · Traditional Respironics New Jersey, Inc.08/09/2011SE
K101348Agachamber SpacerNVP · Traditional Aga Plastic Ind. Com. Ltda.04/29/2011SE

More from Aga Plastic Ind. Com. Ltda.

510(k)DeviceDecision
K122252Space Chamber Plus Compact Space Chamber PlusNVP · Traditional 11/13/2013SE

Questions and answers

When was Antistatic Compact Space Chamber cleared by the FDA?

Antistatic Compact Space Chamber (K143615) received a 510(k) decision of Substantially Equivalent on January 26, 2016, 403 days after the submission was received.

What is the product code of K143615?

The FDA product code is NVP – Holding Chambers, Direct Patient Interface, a Class II (moderate risk) device regulated under 21 CFR 868.5630.