Hoveround Corp. is one of 5210 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hoveround Corp. - FDA 510(k) Cleared Devices
17
Total
15
Cleared
0
Denied
Hoveround Corp. has 15 FDA 510(k) cleared physical medicine devices. Based in Sarasota, US.
Historical record: 15 cleared submissions from 1994 to 2013.
Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.
Hoveround Corp. — FDA 510(k) Products and Clearance History
17 devices
Cleared
May 07, 2013
HOVERROUND TEKNIQUE
Physical Medicine
245d
Cleared
May 07, 2013
HOVEROUND TEKNIQUE
Physical Medicine
242d
Cleared
Mar 26, 2010
HOVEROUND TEKNIQUE, MODEL HD-6
Physical Medicine
30d
Cleared
Mar 22, 2010
HOVEROUND HOVERGLIDE MODEL HOVERGLIDE MK-2
Physical Medicine
89d
Cleared
Mar 22, 2010
HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT
Physical Medicine
38d
Cleared
Mar 19, 2009
HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR
Physical Medicine
63d
Cleared
Dec 03, 2004
HOVEROUND SE-3 POWERCHAIR
Physical Medicine
42d
Cleared
Dec 03, 2004
HOVEROUND E100 POWER CHAIR
Physical Medicine
25d
Cleared
Oct 21, 2004
HOVEROUND MPV-5 POWERCHAIR
Physical Medicine
31d
Cleared
Sep 29, 2004
HOVEROUND POWER WHEELCHAIR, MODEL HD700
Physical Medicine
62d
Cleared
Dec 02, 2002
HOVEROUND REHAB SEATING SYSTEM FOR POWER WHEELCHAIRS
Physical Medicine
84d
Cleared
Apr 19, 2002
TEKNIQUE-HOVEROUND POWER WHEEL CHAIR
Physical Medicine
10d