510(k) Report

FDA product code · Ear, nose and throat

Audiometer

EWOClass II21 CFR 874.1050510(k) exempt235 decisions since 19765 recalls

FDA lists EWO as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 874.9 applies, such as a new intended use or a different fundamental technology. 235 FDA decisions since 1976. 510(k) reviews decided 2021–2025 took a median of 164 days (half between 120 and 198). 5 recalls name this code, 0 of them Class I. The most-cited predicate is K072033, named by 4 later devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, ear, nose and throat panel

Twenty years of EWO at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · EWO

2in 2024

2007: 52008: 12009: 22010: 22011: 32012: 42013: 22014: 12015: 42017: 22018: 22019: 12022: 12023: 12024: 2
2007high 5 (2007) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EWO

173in 2015

2007: 69 days median2011: 151 days median2012: 137 days median2015: 173 days median
2007high 173 (2015) · low 69 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · EWO

4in 2023

2008: 12023: 4
2007high 4 (2023) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EWO

13in 2025

2007: 12008: 12009: 12010: 42011: 22015: 12019: 62020: 72021: 32022: 62023: 32024: 22025: 13
2007high 13 (2025) · low 0 (2012)2025

MAUDE reports naming product code EWO, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200756901
20081—11
20092—01
20102—04
2011315102
2012413700
20132—00
20141—00
2015417301
20160—00
20172—00
20182—00
20191—06
20200—07
20210—03
20221—06
20231—43
20242—02
20250—013
20260—0—
FIG. 1 — EWO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in EWO? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 874.1050.