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FDA 510(k)

MAGSTIM RAPID

K-Number: K992911 · 2000-01-07

ApplicantMagstim Corporation US
Decision Date2000-01-07
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MAGSTIM RAPID is the device name listed in this FDA 510(k) record. The listed applicant is Magstim Corporation US. It received FDA 510(k) clearance on 2000-01-07 under 510(k) number K992911. 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 RAPID?

MAGSTIM RAPID is a medical device that received FDA 510(k) clearance on 2000-01-07. The listed applicant is Magstim Corporation US. The 510(k) number is K992911.

When did MAGSTIM RAPID receive FDA 510(k) clearance?

MAGSTIM RAPID received FDA 510(k) clearance on 2000-01-07, under 510(k) number K992911.

Who is the listed applicant for MAGSTIM RAPID?

The FDA 510(k) record lists Magstim Corporation US as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGSTIM RAPID?

The FDA product code for MAGSTIM RAPID 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.

K263010ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpressinomed Medizintechnik GmbHK253301BraiN20® (BraiN20)Time IS Brain, S.L.K252842SafeOp 3: Neural Informatix SystemAlphatec Spine, Inc.K243982Nicolet EDXNatus Neurology IncorporatedK243495Natus Ultrapro S100 (982A0594)Natus Neurology IncorporatedK242345Delphi StimulatorQuantalx Neuroscience

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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