If you suffer from allergies or sinus congestion, you might want to think twice before using this nasal spray. The U.S. Food and Drug Administration is recalling 89,312 bottles of NasoGel nasal spray ...
We anticipate that IBD Aware will go through an FDA 510(k) regulatory classification as a Class II medical device that will be prescribed by the clinician to the patient, based on their disease ...
EMA establishes regular procedure for scientific advice on certain high-risk medical devices: Amsterdam, The Netherlands Wednesday, February 12, 2025, 13:00 Hrs [IST] EMA, in clos ...
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