# K091940: Magpro, Models R30 with Magoption, X100, X100 with Magoption

- Pathway: 510(k) (Traditional)
- Applicant: Tonica Elektronik A/S
- Decided: Mar 26, 2010 after 269 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
Longest line of descent: 3 generations back to K905059 (1991). 8 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061645: Magpro, Model R30, Tonica Elektronik A/S (2006) Summary page 1.
- K926516: Dantec Magnetic Stimulator Magpro, Dantec Medical, Inc. (1993) Summary page 1.
- K051864: Magstim RAPID2, Magstim Super RAPID2, Models 3004-000, 3005-00, The Magstim Company, Ltd. (2005) Summary page 1.
- K944547: Dantec Keypoint, Mckenna & Cuneo (1995) Summary page 1.
- K051357: DS7A Constant Current High Voltage Stimulator, Model DS7A; DS7AH Constant Current High Voltage Stimulator, Model DS7AH, Digitimer, Ltd. (2005)

## Most influential descendants
- K192823: Mega-TMS (2021), 0 descendants of its own
- K162873: MEP Monitor (2017), 0 descendants of its own

## Indications for use
The devices are intended to be used for stimulation of peripheral nerves for diagnostic purposes.

Source page: https://510kreport.com/device/K091940
Methodology: https://510kreport.com/methodology