Microware, Inc. is one of 24293 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microware, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MICROWARE 200
1
Total
1
Cleared
0
Denied
Microware, Inc. has 1 FDA 510(k) cleared medical devices. Based in Vancouver, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Microware, 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 - Microware, Inc.
1 devices