RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581— 510(k) K090750
Substantially EquivalentRestorative Therapies, Inc.
FDA 510(k) clearance K090750 for RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581, Substantially Equivalent on 2009-08-05. 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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