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FDA grants clearance for Inogen’s SIMEOX 200 airway clearance device
The US Food and Drug Administration (FDA) has granted 510(k) clearance for Inogen’s SIMEOX 200 Airway Clearance Device for individuals suffering from chronic respiratory conditions. The SIMEOX ...
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Inogen Receives FDA 510(k) Clearance for SIMEOX 200 Airway Clearance Device
“By tapping into our well-established network of healthcare providers, B2B partners, and our Direct-to-Patient team, we aim to bring this next-generation airway clearance device to patients ...