510(k) Report

Devices descending from K060032

12 later devices reach RT300-S, Model FA100052; RT300-SP, Model FA100053 through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K073237Rehastim & RehamoveHasomed GmbH20078—
+1K071113RT300-S, Model FA100052, RT300-SP (Pediatric Version), Model FA100053Restorative Therapies, Inc.20077—
+2K112844Rehastim 2, Rehamove 2Hasomed GmbH20112—
+2K090750RT300-SL, Model FA100052; RT300-Slsa, Model FA104581Restorative Therapies, Inc.20094—
+2K071486RT300-S, RT300-SP (Pediatric Version), Model FA100052, FA100053Restorative Therapies, Inc.20076—
+3K162470RT300 FES cycle ergometerRestorative Therapies, Inc.20170—
+3K162683RehaStim 2Hasomed GmbH20170—
+3K160614Xcite Clinical StationRestorative Therapies, Inc.20161—
+3K132416Rehastim 2, Erigopro (Fes)Hasomed GmbH20141—
+3K103370RT200Restorative Therapies, Inc.20110—
+3K103366RT600Restorative Therapies, Inc.20110—
+3K072398RT300-S and RT300-SP Fes Cycle ErgometerRestorative Therapies, Inc.20075—