** Shares of medical device maker Inogen INGN.O rise 10.6%
to $9.49 premarket
** Co says its device for clearing mucus from lungs has
received FDA 510(k) approval
** FDA 510(k) approval is a process where a medical device
is shown to be safe and similar to an existing device before it
can be sold
** The device, SIMEOX 200 Airway Clearance Device, helps
improve bronchial drainage in patients with chronic respiratory
diseases - INGN
** The device is intended for patients who can cough on
their own - INGN
** Co plans a limited launch of the device at targeted sites
in 2025
** As of last close, stock has risen 56.3% YTD
(Reporting by Kamal Choudhury in Bengaluru)
((Kamal.Choudhury@thomsonreuters.com;))