IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2— 510(k) K060975

Substantially Equivalent

Theratech, Inc.

FDA 510(k) clearance K060975 for IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2, Substantially Equivalent on 2006-05-10. Applicant: Theratech, Inc..

Clearance details

Applicant: Theratech, Inc.
Product code: Code LIH
Advisory panel: Neurology
Date received: 2006-04-10
Decision date: 2006-05-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Madison, TN, US

Download summary PDF View on FDA.gov ↗

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