Medical Device Manufacturer · US , Lansing , MI

Talley Group, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1991
6
Total
6
Cleared
0
Denied

Talley Group, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Lansing, US.

Historical record: 6 cleared submissions from 1991 to 2016. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Talley Group, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Talley Group, Ltd.

6 devices
1-6 of 6
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