510(k) Report

FDA product code · Gastroenterology and urology

Kit, Choledochoscope, Flexible And Rigid

NWSClass II21 CFR 876.1500510(k) required1 decision since 19810 recalls

1 FDA decision since 1981. No recall names this code.

Flexible and Rigid Choledochoscope Kit

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 NWS 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 · NWS

FDA has decided no NWS device since 2007.

Median 510(k) review, days · NWS

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

Recalls per year · NWS

No recall names NWS since 2007.

Adverse event reports per year · NWS

No MAUDE report names NWS 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
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — NWS by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NWS? 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 876.1500.