510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823774Substantially Equivalent

Wilson Eustachian Tubal, Sonograph

Antares Technical Associates, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823774 is the FDA 510(k) clearance record for WILSON EUSTACHIAN TUBAL, SONOGRAPH, a class I device, cleared for Antares Technical Associates, Inc. on under FDA product code ETK (Tube, Toynbee Diagnostic). FDA records list one 510(k) clearance for Antares Technical Associates, Inc. As of , FDA records show no recalls naming K823774.

Clearance record

Decision date
Received
(34 days to decision)
Product code
ETK Tube, Toynbee Diagnostic
Regulation
21 CFR 874.1925
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Antares Technical Associates, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ETK

Trailing 12 months

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

FDA records show no clearances under product code ETK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ETK, 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