Medical Device Manufacturer · US , Lansing , MI

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

6 submissions · 6 cleared · Since 1991

Total

Cleared

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.

510(k) submissions have been managed by Sgr Consulting Services as regulatory consultant.

Talley Group, Ltd. is one of 13075 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6