ELECTRONIC PULSE MASSAGER TENS ELECTRONIC PULSE MASSAGER— 510(k) K113544

Name: FDA 510(k) clearance K113544
Creator: U.S. Food and Drug Administration
Published: 2012-07-27

Substantially Equivalent

Prospera Corporation

FDA 510(k) clearance K113544 for ELECTRONIC PULSE MASSAGER TENS ELECTRONIC PULSE MASSAGER, Substantially Equivalent on 2012-07-27. Applicant: Prospera Corporation. Device class: 2.

Clearance details

Applicant: Prospera Corporation
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2011-12-01
Decision date: 2012-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

Download summary PDF View on FDA.gov ↗

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