510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K041853Substantially Equivalent

Otogram

Tympany, Inc., Deer Field IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K041853 is the FDA 510(k) clearance record for OTOGRAM, a class II device, cleared for Tympany, Inc. on under FDA product code ETW (Calibrator, Hearing Aid / Earphone And Analysis Systems). FDA records list 2 510(k) clearances for Tympany, Inc., from to . As of , FDA records show no recalls naming K041853.

Clearance record

Decision date
Received
(57 days to decision)
Product code
ETW Calibrator, Hearing Aid / Earphone And Analysis Systems
Regulation
21 CFR 874.3310
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Tympany, Inc. P.O. Box 7007, Deer Field IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ETW

Trailing 12 months

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

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