Inogen Secures FDA 510(k) Clearance For SIMEOX 200 Airway Clearance Device
Monday announced that the company has received U.S. Food and Drug Administration 510(k) clearance for the SIMEOX ...
Inogen Expands U.S. Market with FDA Clearance
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Inogen Receives FDA 510(k) Clearance for SIMEOX 200 Airway Clearance Device
--(BUSINESS WIRE)--Inogen, Inc. (Nasdaq: INGN), a medical technology company offering innovative respiratory products for use in the homecare setting, today announced that it has received U.S. Food ...