510(k) Report

FDA product code · Ear, nose and throat

Device, Inflation, Middle Ear

MJVClass U510(k) required6 decisions since 19920 recalls

6 FDA decisions since 1992. 510(k) reviews decided 2021–2025 took a median of 82 days (half between 70 and 93). No recall names this code. The most-cited predicate is K951596, named by 1 later device.

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 MJV 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 · MJV

1in 2023

2008: 12021: 12023: 12026 (partial year): 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MJV

Too few MJV 510(k)s in any year since 2007 to give a median.

Recalls per year · MJV

No recall names MJV since 2007.

Adverse event reports per year · MJV

1in 2021

2015: 12017: 12019: 12021: 1
2007high 1 (2015) · low 0 (2007)2025

MAUDE reports naming product code MJV, 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
20070—00
20081—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—01
20160—00
20170—01
20180—00
20190—01
20200—00
20211—01
20220—00
20231—00
20240—00
20250—00
20261—0—
FIG. 1 — MJV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MJV? 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