Medical Device Manufacturer · US , Baltimore , MD

Restorative Therapies, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2005

Total

Cleared

Denied

Restorative Therapies, Inc. has 10 FDA 510(k) cleared neurology devices. Based in Baltimore, US.

Historical record: 10 cleared submissions from 2005 to 2017.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Restorative Therapies, Inc.

10 devices

1-10 of 10

Cleared Jul 11, 2017

RT300 FES cycle ergometer

K162470 · GZI

Neurology · 308d

Cleared Dec 16, 2016

Xcite Clinical Station

K160614 · IPF

Physical Medicine · 288d

RT300-SL, MODEL FA100052

K090750 · GZI

Neurology · 138d

Cleared Nov 21, 2007

RT300-S AND RT300-SP FES CYCLE ERGOMETER

K072398 · GZI

Neurology · 86d

Cleared Sep 10, 2007

RT300-S, RT300-SP (PEDIATRIC VERSION), MODEL FA100052, FA100053

K071486 · GZI

Neurology · 103d

Cleared Jul 05, 2007

RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053

K071113 · GZI

Neurology · 76d

Cleared Mar 10, 2006

RT300-S, MODEL FA100052

K060032 · GZI

Neurology · 64d

Cleared Jun 27, 2005

FES CYCLE ERGOMETER, MODEL RT300-S

K050036 · GZI

Neurology · 171d

Restorative Therapies, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Restorative Therapies, Inc.

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