MAGSTIM 200-2— 510(k) K060847

Name: FDA 510(k) clearance K060847
Creator: U.S. Food and Drug Administration
Published: 2006-09-26

Substantially Equivalent

Magstim Company Us, LLC

FDA 510(k) clearance K060847 for MAGSTIM 200-2, Substantially Equivalent on 2006-09-26. Applicant: Magstim Company Us, LLC. Device class: 2.

Clearance details

Applicant: Magstim Company Us, LLC
Product code: Code GWF
Device class: Class 2
Regulation: 21 CFR 882.1870
Advisory panel: Neurology
Date received: 2006-03-28
Decision date: 2006-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woburn, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GWF

product code GWF

Malfunction: 2,364
Other: 4
Total: 2,368

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.