Anutra Medical, Inc. is one of 19049 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anutra Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANUTRA Feedback Aspiration Syringe
1
Total
1
Cleared
0
Denied
Anutra Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Anutra Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Anutra Medical, Inc.
1 devices