RT300-S AND RT300-SP FES CYCLE ERGOMETER— 510(k) K072398
Substantially EquivalentRestorative Therapies, Inc.
FDA 510(k) clearance K072398 for RT300-S AND RT300-SP FES CYCLE ERGOMETER, Substantially Equivalent on 2007-11-21. Applicant: Restorative Therapies, Inc.. Device class: 2.
Clearance details
- Applicant
- Restorative Therapies, Inc.
- Product code
- Code GZI
- Device class
- Class 2
- Regulation
- 21 CFR 882.5810
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baltimore, MD, US
Recent devices under product code GZI
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