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Home » Guidance Aims to Help Hemostatic Devicemakers Prepare 510(k)s
Guidance Aims to Help Hemostatic Devicemakers Prepare 510(k)s
December 6, 2006
The U.S. FDA has issued a draft guidance to help absorbable hemostatic device manufacturers prepare 510(k)s, following the reclassification of such devices as Class II special controls.
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