Sonovation, Inc. Dba Avr Sonovation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonovation, Inc. Dba Avr Sonovation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sonovation, Inc. Dba Avr Sonovation has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 1991 to 1992. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Sonovation, Inc. Dba Avr Sonovation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sonovation, Inc. Dba Avr Sonovation
2 devices