FDA product code · Gastroenterology and urology

Plier, Tube

Name: FDA decisions, review times, recalls and adverse event reports for product code FJO
Creator: 510(k) Report

FJOClass I21 CFR 876.5540510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

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 FJO 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.

FIG. 1 — FJO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FJO? 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 876.5540.

NFK Kit, Repair, Catheter, Hemodialysis NNE Needle, Fistula, Reprocessed MSD Catheter, Hemodialysis, Implanted LFJ Catheter, Subclavian FJY Plier, Crimp FKA Dilator, Vessel NOO Clamp, Dialysis Arm NYU Catheter, Hemodialysis, Implanted, Coated KNR Adapter, A-V Shunt Or Fistula MPB Catheter, Hemodialysis, Non-Implanted PFH Venous Window Needle Guide FIE Needle, Fistula