CamNtech is pleased to announce that the MotionWatch and PRO-Diary have been cleared by the US FDA to be legally marketed in the USA.

 

CamNtech is pleased to announce that the MotionWatch and PRO-Diary have been cleared by the US FDA to be legally marketed in the USA.

These products join the Actiheart and Actiwave devices to form a full suite of products that may be used for clinical or research applications in the USA.

The MotionWatch and PRO-Diary are US FDA class II devices and are grouped under product code LEL.

CamNtech are committed  to providing professional solutions to clinicians and researchers around the world.

 

UK & International customers

CamNtech Ltd.
Manor Farm
Fenstanton
Cambridgeshire
PE28 9JD, UK

US customers

CamNtech Inc.
630 Boerne Stage Airfield,
Boerne,
Texas 78006,
USA

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VAT No: GB486 3019 34


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