Maxant Technologies, Inc. is one of 22945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Maxant Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDIPORT
1
Total
1
Cleared
0
Denied
Maxant Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Niles, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Maxant Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Maxant Technologies, Inc.
1 devices