Medical Device Manufacturer · US , Little Rock , AR

Keytone Hearing Laboratory - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997
1
Total
1
Cleared
0
Denied

Keytone Hearing Laboratory has 1 FDA 510(k) cleared medical devices. Based in Little Rock, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Keytone Hearing Laboratory Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Keytone Hearing Laboratory

1 devices
1-1 of 1
Filters
All1 Ear, Nose, Throat 1