510(k) Report

FDA product code · General hospital

Air Filter Portable Apparatus

ORCClass II21 CFR 878.5070510(k) required6 decisions since 20110 recalls

6 FDA decisions since 2011. No recall names this code. The most-cited predicate is K153498, named by 2 later devices.

The sytem is intended to control the surgical environment to prevent bacterial contamination during surgical procedures.

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, general hospital panel

Twenty years of ORC 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 · ORC

1in 2019

2011: 12013: 12016: 12017: 22019: 1
2007high 2 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ORC

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

Recalls per year · ORC

No recall names ORC since 2007.

Adverse event reports per year · ORC

No MAUDE report names ORC since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20111—00
20120—00
20131—00
20140—00
20150—00
20161—00
20172—00
20180—00
20191—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — ORC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ORC? 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 878.5070.