Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Restorative Therapies, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K162470	RT300 FES cycle ergometer	GZI	2017-07-11	View
510(k)	K160614	Xcite Clinical Station	IPF	2016-12-16	View
510(k)	K103370	RT200	GZI	2011-04-05	View
510(k)	K103366	RT600	GZI	2011-04-04	View
510(k)	K090750	RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581	GZI	2009-08-05	View
510(k)	K072398	RT300-S AND RT300-SP FES CYCLE ERGOMETER	GZI	2007-11-21	View
510(k)	K071486	RT300-S, RT300-SP (PEDIATRIC VERSION), MODEL FA100052, FA100053	GZI	2007-09-10	View
510(k)	K071113	RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053	GZI	2007-07-05	View
510(k)	K060032	RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053	GZI	2006-03-10	View
510(k)	K050036	FES CYCLE ERGOMETER, MODEL RT300-S	GZI	2005-06-27	View

↑