HORIZON TMS Therapy System
K-Number: K180907 · 2018-08-03
ApplicantMagstim Company, Ltd.
Decision Date2018-08-03
Product CodeOBP
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
HORIZON TMS Therapy System is a medical device manufactured by Magstim Company, Ltd.. It received FDA 510(k) clearance on 2018-08-03 under approval number K180907. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the HORIZON TMS Therapy System?
HORIZON TMS Therapy System is a medical device that received FDA 510(k) clearance on 2018-08-03. It is manufactured by Magstim Company, Ltd.. The 510(k) number is K180907.
When was HORIZON TMS Therapy System approved by the FDA?
HORIZON TMS Therapy System received FDA 510(k) clearance on 2018-08-03, under approval number K180907.
What company makes HORIZON TMS Therapy System?
HORIZON TMS Therapy System is manufactured by Magstim Company, Ltd..
What is the FDA product code for HORIZON TMS Therapy System?
The FDA product code for HORIZON TMS Therapy System is OBP.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.