Cranial electrotherapy stimulator to treat depression
PMA Number: P230024 · 2026-07-14
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Device Summary
Frequently Asked Questions
What is the Cranial electrotherapy stimulator to treat depression?
Cranial electrotherapy stimulator to treat depression is a medical device that received FDA 510(k) clearance on 2026-07-14. The listed applicant is Flow Neuroscience AB.
When did Cranial electrotherapy stimulator to treat depression receive FDA 510(k) clearance?
The clearance date for Cranial electrotherapy stimulator to treat depression can be found in the official FDA records.
Who is the listed applicant for Cranial electrotherapy stimulator to treat depression?
The FDA 510(k) record lists Flow Neuroscience AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cranial electrotherapy stimulator to treat depression?
The FDA product code for Cranial electrotherapy stimulator to treat depression is JXK.
Related Clinical Trials
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.
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