CloudTMS for OCD
K-Number: K221129 · 2023-03-10
Device Summary
Frequently Asked Questions
What is the CloudTMS for OCD?
CloudTMS for OCD is a medical device that received FDA 510(k) clearance on 2023-03-10. The listed applicant is Teleemg, LLC. The 510(k) number is K221129.
When did CloudTMS for OCD receive FDA 510(k) clearance?
CloudTMS for OCD received FDA 510(k) clearance on 2023-03-10, under 510(k) number K221129.
Who is the listed applicant for CloudTMS for OCD?
The FDA 510(k) record lists Teleemg, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CloudTMS for OCD?
The FDA product code for CloudTMS for OCD is QCI.
Other records listing Teleemg, LLC 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: QCI)
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.