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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1715
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dc.contributor.authorGupta, Dr. Divya-
dc.date.accessioned2023-12-14T07:29:24Z-
dc.date.available2023-12-14T07:29:24Z-
dc.date.issued2023-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1715-
dc.language.isoenen_US
dc.publisherIIHMR Delhien_US
dc.titleThe Role of FDA 510k Approval in Clearance of Software as A Medical Deviceen_US
dc.mentorDr. Sumesh Kumaren_US
dc.organizationCurio Digital Therapeuticsen_US
dc.codeS3914en_US
dc.subjectiihmrHealth IT Managementen_US
Appears in Collections:PGDHM BATCH 2021_2023

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Divya Gupta 510k Report (1).pdf1.3 MBAdobe PDFView/Open
divya gupta synopse ppt.pptx1.03 MBMicrosoft Powerpoint XMLView/Open
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