Storz Medical MAGNETOLITH Muscle Stimulator
K-Number: K203710 · 2021-05-03
Device Summary
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. The listed applicant is Storz Medical AG. The 510(k) number is K203710.
When did Storz Medical MAGNETOLITH Muscle Stimulator receive FDA 510(k) clearance?
Storz Medical MAGNETOLITH Muscle Stimulator received FDA 510(k) clearance on 2021-05-03, under 510(k) number K203710.
Who is the listed applicant for Storz Medical MAGNETOLITH Muscle Stimulator?
The FDA 510(k) record lists Storz Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator?
The FDA product code for Storz Medical MAGNETOLITH Muscle Stimulator is IPF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Storz Medical AG as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IPF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.