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..
Clearance details
- Applicant
- Restorative Therapies, Inc.
- Product code
- Code GZI
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baltimore, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.