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FDA 510(k)

MAGSTIM 200-2

K-Number: K060847 · 2006-09-26

ApplicantMagstim Company Us, LLC
Decision Date2006-09-26
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAGSTIM 200-2 is the device name listed in this FDA 510(k) record. The listed applicant is Magstim Company Us, LLC. It received FDA 510(k) clearance on 2006-09-26 under 510(k) number K060847. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGSTIM 200-2?

MAGSTIM 200-2 is a medical device that received FDA 510(k) clearance on 2006-09-26. The listed applicant is Magstim Company Us, LLC. The 510(k) number is K060847.

When did MAGSTIM 200-2 receive FDA 510(k) clearance?

MAGSTIM 200-2 received FDA 510(k) clearance on 2006-09-26, under 510(k) number K060847.

Who is the listed applicant for MAGSTIM 200-2?

The FDA 510(k) record lists Magstim Company Us, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGSTIM 200-2?

The FDA product code for MAGSTIM 200-2 is GWF.

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Related Devices (Code: GWF)

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.

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Official Source

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

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