Fujifilm New Development U.S.A., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fujifilm New Development U.S.A., Inc. - FDA 510(k) Cleared Devices
Recent clearances: EPX-4440FN Digital Video Processor with Light Source
3
Total
3
Cleared
0
Denied
Fujifilm New Development U.S.A., Inc. has 3 FDA 510(k) cleared medical devices. Based in Waltham, US.
Historical record: 3 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fujifilm New Development U.S.A., Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Fujifilm New Development U.S.A., Inc.
3 devices