Precision Biometrics, Inc. is one of 19082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Biometrics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MYOVISION 3.0 WIREFREE SYSTEM
1
Total
1
Cleared
0
Denied
Precision Biometrics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Precision Biometrics, 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 - Precision Biometrics, Inc.
1 devices