# K061645: Magpro, Model R30

- Pathway: 510(k) (Traditional)
- Applicant: Tonica Elektronik A/S
- Decided: Oct 31, 2006 after 141 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: 2 generations back to K905059 (1991). 4 ancestors in all.
7 later devices descend from it; 5 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- 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.

## Most influential descendants
- K091940: Magpro, Models R30 with Magoption, X100, X100 with Magoption (2010), 2 descendants of its own
- K160280: MagPro R20 (2016), 1 descendant of its own
- K242345: Delphi Stimulator (2024), 0 descendants of its own
- K192823: Mega-TMS (2021), 0 descendants of its own
- K162873: MEP Monitor (2017), 0 descendants of its own

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

Source page: https://510kreport.com/device/K061645
Methodology: https://510kreport.com/methodology