Be Technologies, Inc. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Be Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Uroflowmeter
1
Total
1
Cleared
0
Denied
Be Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Be Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Be Technologies, Inc.
1 devices