Talley Group, Ltd. is one of 4831 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Talley Group, Ltd. - FDA 510(k) Cleared Devices
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
Cleared
Feb 19, 2016
Venturi Gauze Wound Care Sets with Portal Drain
General & Plastic Surgery
282d
Cleared
Jan 05, 2016
VENTURI MiNO TG600/14
General & Plastic Surgery
442d
Cleared
Apr 10, 1992
TALLEY MICRO SYSTEM/TALLEY RIPPLEBED
General Hospital
170d
Cleared
Feb 11, 1992
MULTIPULSE SEQUENTIAL COMPRESSION UNIT
Physical Medicine
111d
Cleared
Dec 19, 1991
OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITOR
Physical Medicine
57d
Cleared
Dec 19, 1991
TALLEY SD.500 SKIN PRESSURE EVALUATOR
Physical Medicine
57d