510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN240064Unknown

CT-132

Click Therapeutics, Inc., New York NY / Direct, Unknown
FDA source (opens on fda.gov)

DEN240064 is the FDA 510(k) clearance record for CT-132, a class II device, cleared for Click Therapeutics, Inc. on under FDA product code SEE (Computerized Behavioral Therapy Device For Migraine). FDA's definition for product code SEE 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". FDA records list 2 510(k) clearances for Click Therapeutics, Inc., from to . As of , FDA records show no recalls naming DEN240064.

Clearance record

Decision date
Received
(150 days to decision)
Product code
SEE Computerized Behavioral Therapy Device For Migraine
Regulation
21 CFR 882.5806
Device class
Class II
Review panel
Neurology
Applicant
Click Therapeutics, Inc. 80 White St., New York NY
Third party review
No

Clearances, product code SEE

Trailing 12 months

FDA records hold no clearances under product code SEE in the trailing twelve months.

FDA records show no clearances under product code SEE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code SEE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260