The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
The U.S. Food and Drug Administration (FDA) has given its second most serious risk level, Class II, to a product from D. Coluccio & Sons. The recalled product is a 300 gram pack of chocolate chip ...
20h
Hosted on MSNFDA grants orphan drug status to Arbor Biotechnologies’ PH1The US Food and Drug Administration (FDA) has granted orphan drug designation (ODD) and rare paediatric disease designation (RPDD) to Arbor Biotechnologies' gene editing therapeutic, ABO-101, to treat ...
The U.S. Food and Drug Administration has approved Onapgo (apomorphine hydrochloride) injection as the first and only ...
A device long used by adults to manage migraines was now available for children as young as eight years old, offering new ...
23h
Hosted on MSNNewronika secures FDA’s IDE to begin adaptive deep brain stimulation system trialThe trial will assess the efficacy and safety of the system in individuals with movement disorders such as Parkinson's disease.
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