510(k) Report

FDA product code · Ear, nose and throat

Pillow, Cervical (For Mild Sleep Apnea)

MYBClass II21 CFR 872.5570510(k) required6 decisions since 19990 recalls

6 FDA decisions since 1999. No recall names this code. The most-cited predicate is K023010, named by 2 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 MYB 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 · MYB

1in 2018

2010: 12014: 12018: 1
2007high 1 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MYB

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

Recalls per year · MYB

No recall names MYB since 2007.

Adverse event reports per year · MYB

1in 2025

2007: 22025: 1
2007high 2 (2007) · low 0 (2008)2025

MAUDE reports naming product code MYB, 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—02
20080—00
20090—00
20101—00
20110—00
20120—00
20130—00
20141—00
20150—00
20160—00
20170—00
20181—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—01
20260—0—
FIG. 1 — MYB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MYB? 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 872.5570.