Stentor, Inc. is one of 25288 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stentor, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ISITE PACS, ISITE RADIOLOGY, STENTOR, PAGEVIEW
3
Total
3
Cleared
0
Denied
Stentor, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Historical record: 3 cleared submissions from 1999 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Stentor, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Product Service, Inc. and Tuv America, Inc..
FDA 510(k) Regulatory Record - Stentor, Inc.
3 devices