INTERFERENTIAL STIMULATOR, MODEL RTM1000— 510(k) K030254

Name: FDA 510(k) clearance K030254
Creator: U.S. Food and Drug Administration
Published: 2003-02-26

Substantially Equivalent

Ryan Telemedicine

FDA 510(k) clearance K030254 for INTERFERENTIAL STIMULATOR, MODEL RTM1000, Substantially Equivalent on 2003-02-26. Applicant: Ryan Telemedicine. Device class: 2.

Clearance details

Applicant: Ryan Telemedicine
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2003-01-24
Decision date: 2003-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Costa Mesa, CA, US

Download summary PDF View on FDA.gov ↗

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