Vbox, Inc. is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vbox, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TROOPER OXYGEN CONCENTRATOR
1
Total
1
Cleared
0
Denied
Vbox, Inc. has 1 FDA 510(k) cleared medical devices. Based in White Bear Lake, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vbox, 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 - Vbox, Inc.
1 devices