510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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SEEClass II

Computerized Behavioral Therapy Device For Migraine

21 CFR 882.5806 / Neurology
FDA source (opens on fda.gov)

SEE is the FDA product code for Computerized Behavioral Therapy Device For Migraine, a class II device type, regulated under 21 CFR 882.5806. FDA's definition for this code reads: "A computerized behavioral therapy device for headache is a prescription device intended to provide a computerized version of behavioral therapy for the treatment of headache". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
SEE
Device name
Computerized Behavioral Therapy Device For Migraine
FDA definition
A computerized behavioral therapy device for headache is a prescription device intended to provide a computerized version of behavioral therapy for the treatment of headache.
Regulation
21 CFR 882.5806
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code SEE

By decision year
1 clearance under product code SEE with a decision year between 2025 and 2025, 2025 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code SEE by decision year
YearClearances
20251

Applicants with the most clearances

Product code SEE
Applicants holding the most 510(k) clearances under product code SEE
ApplicantClearances
Click Therapeutics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code