A-M Systems, Inc. is one of 23742 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A-M Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: A-M SYSTEMS VIROMAX VIRAL AND BACTERIAL FILTER, VBMAX
2
Total
2
Cleared
0
Denied
A-M Systems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Carlsborg, US.
Historical record: 2 cleared submissions from 2000 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by A-M Systems, 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 - A-M Systems, Inc.
2 devices