The Magstim Company , Ltd.
The Magstim Company , Ltd. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2023.
Top product codes for The Magstim Company , Ltd.
Recent clearances by The Magstim Company , Ltd.
- K232235 — Magstim®Horizon® 3.0 TMS Therapy System +4 more
- K130403 — MAGSTIM DOUBLE 70-2 COIL
- K083242 — NEUROSIGN AVALANCHE MOTOR NERVE MONITOR
- K080499 — MAGSTIM DOUBLE 70MM AIR FILM COIL, MODEL 3910-00
- K071349 — NEUROSIGN LARYNGEAL ELECTRODES
- K051864 — MAGSTIM RAPID2, MAGSTIM SUPER RAPID2, MODELS 3004-000, 3005-00
- K053141 — NEUROSIGN MOTOR NERVE MONITOR, MODELS NEUROSIGN 400 & 800
- K991583 — NEUROSIGN 400, 4 CHANNEL MOTOR NERVE MONITOR
- K980148 — NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR
- K964869 — NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR
- K945799 — NEUROSIGN 100 IMPEDANCE METER
- K951641 — NEUROSCREEN SOFTWARE FOR USE WITH THE NEUROSIGN 100 NERVE MONITOR
- K923056 — NEUROSIGN MODEL 100
Data sourced from openFDA. This site is unofficial and independent of the FDA.