510(k) Report

FDA product code · Gastroenterology and urology

Endoscopic Contamination Prevention Sheath

ODBClass II21 CFR 876.1500510(k) required5 decisions since 19940 recalls

5 FDA decisions since 1994. No recall names this code. The most-cited predicate is K080550, named by 1 later device.

To protect an endoscope from contamination by providing a barrier between the body and the endoscope.

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, gastroenterology and urology panel

Twenty years of ODB 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 · ODB

1in 2019

2008: 12016: 12019: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODB

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

Recalls per year · ODB

No recall names ODB since 2007.

Adverse event reports per year · ODB

10in 2025

2016: 32017: 22019: 62020: 52022: 22023: 82024: 22025: 10
2007high 10 (2025) · low 0 (2007)2025

MAUDE reports naming product code ODB, 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—00
20161—03
20170—02
20180—00
20191—06
20200—05
20210—00
20220—02
20230—08
20240—02
20250—010
20260—0—
FIG. 1 — ODB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

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

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Related product codes

Other codes under 21 CFR 876.1500.