AUSTRALIA TGA (2015) - ADVISORY COMMITTEE ON THE SAFETY OF MEDICAL DEVICES

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• The Australian TGA Advisory Committee on the Safety of Medical Devices, "cancelled" the registration and certification of all soft 'mild' hyperbaric chambers.​​

 

 * Sellers and therapists providing soft and mild HBOT systems to the public must be aware that they may be subject to "criminal prosecution" under the TGA and ACCC for unregistered chamber sales and 'risks to public safety'.

 

• https://www.tga.gov.au/publication-issue/medical-devices-safety-update-volume-3-number-6-november-2015

• TGA policy on cancelled products - ​recalling products from the market

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