510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K853271Substantially Equivalent

Hearing Aid Analysis System

Robert Bosch Corp., St. James NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853271 is the FDA 510(k) clearance record for HEARING AID ANALYSIS SYSTEM, a class II device, cleared for Robert Bosch Corp. on under FDA product code ETW (Calibrator, Hearing Aid / Earphone And Analysis Systems). FDA records list 21 510(k) clearances for Robert Bosch Corp., from to . As of , FDA records show no recalls naming K853271.

Clearance record

Decision date
Received
(164 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
Robert Bosch Corp. Flower Field Bldg. #17, St. James NY
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