MarketWatch25 天
Inogen Gets FDA Clearance for Airway Clearance Device
Inogen said regulators have cleared its SIMEOX 200 Airway Clearance Device to be used by U.S. patients with chronic respiratory diseases. The medical technology company said Monday that the Food ...
News Medical18 天
Inogen receives FDA 510(k) clearance for SIMEOX 200 airway clearance device
clearance for the SIMEOX 200 Airway Clearance Device, expanding the company’s ability to market and meet the various needs of patients with chronic respiratory diseases in the U.S. SIMEOX 200 is ...
来自MSN24 天
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 ...
Nasdaq24 天
Inogen Stock Rises as FDA Clears SIMEOX 200 Airway Clearance Device
Inogen, Inc. INGN recently announced the FDA 510(k) clearance for the SIMEOX 200 Airway Clearance Device. The clearance is likely to expand INGN’s ability to market the device and meet the ...
Business Wire25 天
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 ...
Business Insider25 天
Inogen Secures FDA 510(k) Clearance For SIMEOX 200 Airway Clearance Device
clearance for the SIMEOX 200 Airway Clearance Device, designed to help patients with chronic lung diseases associated with mucus hypersecretion and mucus retention. The device promotes and ...