Seventh Sense Biosystems, Inc. is one of 14053 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seventh Sense Biosystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TAP Blood Collection Device, TAP Blood Collection Device
2
Total
2
Cleared
0
Denied
Seventh Sense Biosystems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Medford, US.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Seventh Sense Biosystems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sharon Timberlake Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Seventh Sense Biosystems, Inc.
2 devices