| http://www.w3.org/ns/prov#value | - ???premarketing and post-marketing regulatory controls.??? Under the FD&C Act, a medical device is:An instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including a component part, or accessory which is:recognized in the official National Formulary, or the United States Pharmacopoeia, or any supplement to them,intended for use in
|
