Medical Device Manufacturer · US , Mchenry , IL

Danavox, Inc. - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 1977
26
Total
26
Cleared
0
Denied

Danavox, Inc. has 26 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.

Historical record: 26 cleared submissions from 1977 to 1994.

Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Danavox, Inc.

26 devices
1-12 of 26
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