Accuthera, Inc. is one of 145 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Accuthera, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CygneX I System
1
Total
1
Cleared
0
Denied
Accuthera, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kawasaki, JP.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Accuthera, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Quality and Regulatory Services, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Accuthera, Inc.
1 devices