Theragenics Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Theragenics Corp. has 5 FDA 510(k) cleared medical devices. Based in Atlanta, US.
Historical record: 5 cleared submissions from 1987 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Theragenics Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jan 03, 2011
I-SEED
Radiology
52d
Cleared
Sep 26, 2007
POIINT OF CARE STRANDING SYSTEM, MODE 1004-00
Radiology
40d
Cleared
Jan 26, 2005
THERALOAD CUSTOM LOADED NEEDLES, MODELS 200 AND 125.S06
Radiology
28d
Cleared
Apr 26, 2001
THERASEED(R) PALLADIUM-103 IMPLANT
Radiology
86d
Cleared
Dec 22, 1987
MODIFIED PALLADIUM SEED MODEL 100
Radiology
29d