{
    "@context": "https://schema.org",
    "@type": "Article",
    "headline": "FDA Proposes Framework for Regulating Software as a Medical Device",
    "url": "https://www.lexblog.com/2017/12/19/fda-proposes-framework-for-regulating-software-as-a-medical-device/",
    "identifier": {
        "@type": "PropertyValue",
        "name": "LexBlog Library record",
        "value": "LEX-WK-DGACPMFW",
        "url": "https://www.lexblog.com/lib/DGACPMFW/"
    },
    "datePublished": "2017-12-19T17:01:29-05:00",
    "dateModified": "2022-07-22T16:58:24-04:00",
    "author": {
        "@type": "Person",
        "name": "Jennifer Pike, Yetunde Oni"
    },
    "sourceOrganization": {
        "@type": "Organization",
        "name": "Reed Smith LLP"
    },
    "organizationScope": "at-publication",
    "isPartOf": "Health Industry Washington Watch",
    "about": "Health Care and Life Sciences",
    "sourceUrl": "https://www.healthindustrywashingtonwatch.com/?p=18141",
    "sourceStability": "may-move"
}