Vgbio, Inc (Dba Physiq) is one of 22807 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vgbio, Inc (Dba Physiq) - FDA 510(k) Cleared Devices
Recent clearances: Personalized Physiology Analytics Engine software
1
Total
1
Cleared
0
Denied
Vgbio, Inc (Dba Physiq) has 1 FDA 510(k) cleared medical devices. Based in Naperville, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vgbio, Inc (Dba Physiq) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vgbio, Inc (Dba Physiq)
1 devices