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INSPIRA™ ART100 Receives FDA 510(k) Clearance
Inspira Technologies OXY announced that its INSPIRA™ ART100 Cardiopulmonary Bypass System has received 510(k) class II clearance from the FDA. The FDA clearance is a significant milestone for the company, suggesting technological and innovative advancements. CEO Dagi Ben Noon and Chairman Professor Benad Goldwasser expressed their appreciation for investors and partners and highlighted the strategic importance of this clearance.
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