FDA 510(k) Applications Submitted by Andrew Barriskill
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060032 |
01/05/2006 |
RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053 |
RESTORATIVE THERAPIES INC. |
K050036 |
01/07/2005 |
FES CYCLE ERGOMETER, MODEL RT300-S |
RESTORATIVE THERAPIES INC. |
K160614 |
03/03/2016 |
Xcite Clinical Station |
RESTORATIVE THERAPIES INC. |
K090750 |
03/20/2009 |
RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581 |
RESTORATIVE THERAPIES INC. |
K071113 |
04/20/2007 |
RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053 |
RESTORATIVE THERAPIES INC. |
K071486 |
05/30/2007 |
RT300-S, RT300-SP (PEDIATRIC VERSION), MODEL FA100052, FA100053 |
RESTORATIVE THERAPIES INC. |
K072398 |
08/27/2007 |
RT300-S AND RT300-SP FES CYCLE ERGOMETER |
RESTORATIVE THERAPIES INC. |
K162470 |
09/06/2016 |
RT300 FES cycle ergometer |
Restorative Therapies, Inc. |
K103370 |
11/17/2010 |
RT200 |
RESTORATIVE THERAPIES INC. |
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