510(k) Report

FDA product code · Gastroenterology and urology

Fluid Jet Removal System

PZPClass II21 CFR 876.4350510(k) required9 decisions since 20170 recalls

9 FDA decisions since 2017. 510(k) reviews decided 2021–2025 took a median of 152 days (half between 102 and 179). No recall names this code. The most-cited predicate is K231024, named by 2 later devices.

The system is used for removal of prostate tissue with a fluid jet.

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 PZP 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 · PZP

1in 2025

2017: 12021: 22023: 12024: 22025: 12026 (partial year): 2
2007high 2 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PZP

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

Recalls per year · PZP

No recall names PZP since 2007.

Adverse event reports per year · PZP

290in 2025

2018: 142019: 702020: 852021: 992022: 1742023: 2542024: 3092025: 290
2007high 309 (2024) · low 0 (2007)2025

MAUDE reports naming product code PZP, 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
20140—00
20150—00
20160—00
20171—00
20180—014
20190—070
20200—085
20212—099
20220—0174
20231—0254
20242—0309
20251—0290
20262—0—
FIG. 1 — PZP by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in PZP? 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