Intuity Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intuity Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POGO Automatic Blood Glucose Monitoring System
3
Total
3
Cleared
0
Denied
Intuity Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 3 cleared submissions from 2016 to 2018. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Intuity Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Intuity Medical, Inc.
3 devices