Accelerated Rehab Designs, Inc. is one of 12239 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accelerated Rehab Designs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: T-2000-POWER TILT SEATING SYSTEM, MODELS ARD-TSTORM, ARD-TP-320, ARD-TG424, ARD-TS525, ARD-TJAZZY, ARD-TLANCER, E-2000 POWER ELEVATING SEAT SYSTEM, MODELS ARD-ESTORM, ARD-EP320, ARD-ELANCER
4
Total
4
Cleared
0
Denied
Accelerated Rehab Designs, Inc. has 4 FDA 510(k) cleared medical devices. Based in Pinehurst, US.
Historical record: 4 cleared submissions from 2000 to 2001. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Accelerated Rehab Designs, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accelerated Rehab Designs, Inc.
4 devices
Cleared
Aug 01, 2001
TRS-2000 POWER TILT/POWER RECLINE SYSTEM
Physical Medicine
12d
Cleared
Jan 12, 2001
TE-2000 POWER TILT/POWER ELEVATING SEAT COMBINATION SYSTEM
Physical Medicine
10d
Cleared
Feb 03, 2000
T-2000-POWER TILT SEATING SYSTEM, MODELS ARD-TSTORM, ARD-TP-320, ARD-TG424,...
Physical Medicine
168d
Cleared
Feb 03, 2000
E-2000 POWER ELEVATING SEAT SYSTEM, MODELS ARD-ESTORM, ARD-EP320, ARD-ELANCER
Physical Medicine
164d