Digitalcore Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Digitalcore Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ONIS-PACS
1
Total
1
Cleared
0
Denied
Digitalcore Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Digitalcore Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Voisin Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Digitalcore Co., Ltd.
1 devices