FDA clears Zephyr's latest update to MATRx plus

By DrBicuspid Staff

November 30, 2020 -- The U.S. Food and Drug Administration (FDA) has granted 510(k) clearance to medical device company Zephyr Sleep Technologies' latest update to MATRx plus.

The clearance eliminates the requirement for a nasal cannula during a sleep theranostic test and makes setting up the take-home Treatment Planning test simpler. Patients now only need a single fingertip pulse oximetry probe for the test.

All existing MATRx plus users who are Connected Program subscribers will receive the update at no additional charge.


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