Anatomage, Inc. is one of 18478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anatomage, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InVivo Web Viewer, CephSimulation, Collage
6
Total
6
Cleared
0
Denied
Anatomage, Inc. has 6 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 6 cleared submissions from 2007 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Anatomage, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Anatomage, Inc.
6 devices