# K060847: Magstim 200-2

- Pathway: 510(k) (Traditional)
- Applicant: Magstim Company Us, LLC
- Decided: Sep 26, 2006 after 182 days
- Product code: GWF (Stimulator, Electrical, Evoked Response)
- Device class: 2
- Regulation: 21 CFR 882.1870
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K192823: Mega-TMS (2021), 0 descendants of its own
- K130403: Magstim Double 70-2 Coil (2013), 0 descendants of its own
- K080499: Magstim Double 70MM Air Film Coil, Model 3910-00 (2008), 0 descendants of its own

## Indications for use
Stimulation of peripheral nerves for diagnostic purposes.

Source page: https://510kreport.com/device/K060847
Methodology: https://510kreport.com/methodology