510(k) Report

FDA product code · General hospital

Gown, Non-Sterile, Non-Isolation, Intended To Provide Moderate Or High Barrier Protection

QPCClass II21 CFR 878.4040510(k) required12 decisions since 20170 recalls

12 FDA decisions since 2017. 510(k) reviews decided 2021–2025 took a median of 207 days (half between 128 and 319). No recall names this code. The most-cited predicate is K160337, named by 3 later devices.

A non-sterile, non-isolation gown intended to be worn by healthcare personnel to provide moderate or high barrier protection in non-sterile and non patient isolation situations. Gowns with antimicrobial/antiviral agents or claims are excluded.

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 QPC 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 · QPC

2in 2025

2017: 12019: 12021: 22022: 12023: 22024: 12025: 22026 (partial year): 2
2007high 2 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QPC

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

Recalls per year · QPC

No recall names QPC since 2007.

Adverse event reports per year · QPC

No MAUDE report names QPC 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
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20171—00
20180—00
20191—00
20200—00
20212—00
20221—00
20232—00
20241—00
20252—00
20262—0—
FIG. 1 — QPC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QPC? 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 878.4040.