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FDA 510(k)

Storz Medical MAGNETOLITH Muscle Stimulator

K-Number: K203710 · 2021-05-03

ApplicantStorz Medical AG
Decision Date2021-05-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Storz Medical MAGNETOLITH Muscle Stimulator is a medical device manufactured by Storz Medical AG. It received FDA 510(k) clearance on 2021-05-03 under approval number K203710. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Storz Medical MAGNETOLITH Muscle Stimulator?

Storz Medical MAGNETOLITH Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2021-05-03. It is manufactured by Storz Medical AG. The 510(k) number is K203710.

When was Storz Medical MAGNETOLITH Muscle Stimulator approved by the FDA?

Storz Medical MAGNETOLITH Muscle Stimulator received FDA 510(k) clearance on 2021-05-03, under approval number K203710.

What company makes Storz Medical MAGNETOLITH Muscle Stimulator?

Storz Medical MAGNETOLITH Muscle Stimulator is manufactured by Storz Medical AG.

What is the FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator?

The FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator is IPF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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