Powered Muscle Stimulator

FDA 510(k) K922529 · M.S.P. , Ltd.

Substantially Equivalent

510(k) numberK922529

Submission

Device name
Powered Muscle Stimulator
Applicant
M.S.P. , Ltd.
Lenexa, KS, US
Received
May 28, 1992
Decision date
November 16, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LIH – Interferential Current Therapy
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

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More from Well-Life Healthcare Limited

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K925680Lsi System IV Interferential,Muscle StimulatorIPF · Traditional 03/02/1993SE
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Questions and answers

When was Powered Muscle Stimulator cleared by the FDA?

Powered Muscle Stimulator (K922529) received a 510(k) decision of Substantially Equivalent on November 16, 1992, 172 days after the submission was received.

What is the product code of K922529?

The FDA product code is LIH – Interferential Current Therapy, a Class II (moderate risk) device regulated under 21 CFR 882.5890.