510(k) Report

FDA product code · Gastroenterology and urology

System, Water Purification, General Medical Use

NHVClass II21 CFR 876.5665510(k) required12 decisions since 20020 recalls

12 FDA decisions since 2002. 510(k) reviews decided 2021–2025 took a median of 267 days (half between 267 and 267). No recall names this code. The most-cited predicate is K141731, named by 3 later devices.

The device is a portable water treatment system which features components and technology similar to water treatment systems previously cleared for hemodialysis. The difference lies with the intended use, as the proposed device is not intended for use in hemodialysis applications, for which a product code currently exists. Instead, the proposed device is intended for use to purify water for general purposes…

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 NHV 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 · NHV

1in 2023

2014: 12016: 42017: 12018: 12019: 22023: 12026 (partial year): 1
2007high 4 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHV

203in 2016

2016: 203 days median
2007high 203 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · NHV

No recall names NHV since 2007.

Adverse event reports per year · NHV

1in 2025

2017: 12018: 22019: 12022: 42025: 1
2007high 4 (2022) · low 0 (2007)2025

MAUDE reports naming product code NHV, 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
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20141—00
20150—00
2016420300
20171—01
20181—02
20192—01
20200—00
20210—00
20220—04
20231—00
20240—00
20250—01
20261—0—
FIG. 1 — NHV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NHV? 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 876.5665.