510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770938Substantially Equivalent

Tinnitus Aid, Model S244

Vicon Instrument Co., MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770938 is the FDA 510(k) clearance record for TINNITUS AID, MODEL S244, a class II device, cleared for Vicon Instrument Co. on under FDA product code KLW (Masker, Tinnitus). FDA records list 8 510(k) clearances for Vicon Instrument Co., from to . As of , FDA records show no recalls naming K770938.

Clearance record

Decision date
Received
(36 days to decision)
Product code
KLW Masker, Tinnitus
Regulation
21 CFR 874.3400
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Vicon Instrument Co.
Third party review
No

Clearances, product code KLW

Trailing 12 months
2 clearances under product code KLW in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KLW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20261
September 20260
October 20260