VitalStim(R) Plus Electrotherapy System

FDA 510(k) K153224 · Djo, LLC

Substantially Equivalent

510(k) numberK153224

Submission

Device name
VitalStim(R) Plus Electrotherapy System
Applicant
Djo, LLC
Vista, CA, US
Received
November 6, 2015
Decision date
February 17, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IPF – Stimulator, Muscle, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5850
Specialty
Physical Medicine

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Questions and answers

When was VitalStim(R) Plus Electrotherapy System cleared by the FDA?

VitalStim(R) Plus Electrotherapy System (K153224) received a 510(k) decision of Substantially Equivalent on February 17, 2016, 103 days after the submission was received.

What is the product code of K153224?

The FDA product code is IPF – Stimulator, Muscle, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5850.