The Role of FDA 510k Approval in Clearance of Software as A Medical Device
| dc.code | S3914 | en_US |
| dc.contributor.author | Gupta, Dr. Divya | |
| dc.date.accessioned | 2023-12-14T07:29:24Z | |
| dc.date.available | 2023-12-14T07:29:24Z | |
| dc.date.issued | 2023 | |
| dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/1715 | |
| dc.language.iso | en | en_US |
| dc.mentor | Dr. Sumesh Kumar | en_US |
| dc.organization | Curio Digital Therapeutics | en_US |
| dc.publisher | IIHMR Delhi | en_US |
| dc.subjectiihmr | Health IT Management | en_US |
| dc.title | The Role of FDA 510k Approval in Clearance of Software as A Medical Device | en_US |