Breezing Med

FDA 510(k) K200076 · Tf Health Co.

Substantially Equivalent

510(k) numberK200076

Submission

Device name
Breezing Med
Applicant
Tf Health Co.
Tempe, AZ, US
Received
January 14, 2020
Decision date
September 25, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BZL – Computer, Oxygen-Uptake
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1730
Specialty
Anesthesiology

Other 510(k)s with product code BZL

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K190561Nicu V'02BZL · Traditional Cosmed Nordic Aps09/04/2020SE
K110810Anascient Breath MonitorBZL · Traditional Invoy Technologies, LLC06/21/2011SE
K093080Metaphor Metabolic MonitorBZL · Traditional Treymed, Inc.01/22/2010SE
K071533Fitmate SeriesBZL · Traditional Cosmed Srl09/28/2007SE
K070858Express SeriesBZL · Special Medical Graphics Corp.04/16/2007SE
K061731Medgraphics Ultima SystemBZL · Special Medical Graphics Corp.09/06/2006SE
K021490Reevue Indirect Calorimeter, MODEL#8100BZL · Traditional Korr Medical Technologies, Inc.01/02/2003SE
K021605MedgemBZL · Special Healthetech, Inc.06/14/2002SE
K010577Bodygem, Model HB211BZL · Traditional Healthetech, Inc.01/10/2002SE
K954731Oxylog 2BZL · Traditional P.K. Morgan , Ltd.01/06/1997SE

Questions and answers

When was Breezing Med cleared by the FDA?

Breezing Med (K200076) received a 510(k) decision of Substantially Equivalent on September 25, 2020, 255 days after the submission was received.

What is the product code of K200076?

The FDA product code is BZL – Computer, Oxygen-Uptake, a Class II (moderate risk) device regulated under 21 CFR 868.1730.