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Restorative Therapies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162470RT300 FES cycle ergometerJuly 11, 2017
K160614Xcite Clinical StationDecember 16, 2016
K103370RT200April 5, 2011
K103366RT600April 4, 2011
K090750RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581August 5, 2009
K072398RT300-S AND RT300-SP FES CYCLE ERGOMETERNovember 21, 2007
K071486RT300-S, RT300-SP (PEDIATRIC VERSION), MODEL FA100052, FA100053September 10, 2007
K071113RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053July 5, 2007
K060032RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053March 10, 2006
K050036FES CYCLE ERGOMETER, MODEL RT300-SJune 27, 2005