RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053— 510(k) K060032

Substantially Equivalent

Restorative Therapies, Inc.

FDA 510(k) clearance K060032 for RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053, Substantially Equivalent on 2006-03-10. Applicant: Restorative Therapies, Inc..

Clearance details

Applicant: Restorative Therapies, Inc.
Product code: Code GZI
Advisory panel: Neurology
Date received: 2006-01-05
Decision date: 2006-03-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Baltimore, MD, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.