510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K060847Substantially Equivalent

Magstim 200-2

Magstim Company Us, LLC, Woburn MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060847 is the FDA 510(k) clearance record for MAGSTIM 200-2, a class II device, cleared for Magstim Company Us, LLC on under FDA product code GWF (Stimulator, Electrical, Evoked Response). FDA records list one 510(k) clearance for Magstim Company Us, LLC. As of , FDA records show no recalls naming K060847.

Clearance record

Decision date
Received
(182 days to decision)
Product code
GWF Stimulator, Electrical, Evoked Response
Regulation
21 CFR 882.1870
Device class
Class II
Review panel
Neurology
Applicant
Magstim Company Us, LLC 304 Cambridge Rd., Woburn MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWF

Trailing 12 months
3 clearances under product code GWF in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260