Apollo TMS Therapy System
K-Number: K232639 · 2024-05-24
Device Summary
Frequently Asked Questions
What is the Apollo TMS Therapy System?
Apollo TMS Therapy System is a medical device that received FDA 510(k) clearance on 2024-05-24. The listed applicant is Mag & More GmbH. The 510(k) number is K232639.
When did Apollo TMS Therapy System receive FDA 510(k) clearance?
Apollo TMS Therapy System received FDA 510(k) clearance on 2024-05-24, under 510(k) number K232639.
Who is the listed applicant for Apollo TMS Therapy System?
The FDA 510(k) record lists Mag & More GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apollo TMS Therapy System?
The FDA product code for Apollo TMS Therapy System is OBP.
Other records listing Mag & More GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OBP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.