Chattanooga Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chattanooga Group - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Chattanooga Group has 11 FDA 510(k) cleared physical medicine devices. Based in Hixson, US.
Historical record: 11 cleared submissions from 2002 to 2009.
Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chattanooga Group
11 devices
Cleared
Jun 01, 2009
COMPEX REHAB
Physical Medicine
84d
Cleared
Mar 18, 2009
INTELECT SWD 100, MODEL 1600
Physical Medicine
118d
Cleared
Feb 09, 2009
COMPEX SPORT PLUS
Physical Medicine
109d
Cleared
Jun 11, 2007
VITALSTIM EXPERIA
Physical Medicine
118d
Cleared
Feb 24, 2006
TRITON/TRU-TRAC/TX/TRITON DTS TRACTION
Physical Medicine
99d
Cleared
Sep 21, 2005
TRITON/TRU-TRAC/TX TRACTION DEVICES
Physical Medicine
65d
Cleared
Sep 08, 2004
VECTRA GENISYS (MODULE & TRANSPORTABLE) AND INTELECT XT (MODULE &...
Physical Medicine
180d
Cleared
Apr 12, 2004
VECTRA TRANSPORTABLE COMBO AND STIM (SPECIALTY LINE DEALERS)
Physical Medicine
66d
Cleared
Dec 11, 2003
VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM
Physical Medicine
251d
Cleared
Dec 03, 2003
VECTRA (INTELECT) EPR ULTRASOUND
Physical Medicine
239d
Cleared
Dec 06, 2002
VITAL STIM
Physical Medicine
60d