510(k) Report

510(k) · Decided

Decided

UPJ Occlusion Balloon Catheter

K183323510(k) TraditionalDecided Aug 5, 2019248-day reviewClass II21 CFR 876.5130

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Cook Incorporated · EYB Catheter, Ureteral, Gastro-Urology

Cleared on Aug 5, 2019 as substantially equivalent to K133750 (Boston Scientific Corporation, 2014) after a 248-day review. Its family tree reaches back 2 generations to 1984.

Decided
Aug 5, 2019
Review
248 days
Class
Class II
Product code
EYB
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K841941 (1984). No later device cites it as a predicate yet.

  1. Root · 2 generations backK841941 Van-Tec Occlusion Balloon CatheterVan-Tec, Inc. · 1984
  2. 1 generation backK133750 Occluder Occlusion Balloon CatheterBoston Scientific Corporation · 2014
  3. This deviceK183323 UPJ Occlusion Balloon CatheterCook Incorporated · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K841941Van-Tec Occlusion Balloon CatheterVan-Tec, Inc.1984—
−1K133750Occluder Occlusion Balloon CatheterBoston Scientific Corporation2014—
0 (this device)K183323UPJ Occlusion Balloon CatheterCook Incorporated2019—
FIG. 1 — Lineage of K183323, 1984–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EYB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new EYB device

  1. #1 K192183 RocaTub Ureteral Catheterscore -0.2 · 3 generations · no Class I recall
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K133750Occluder Occlusion Balloon Catheter
Summary page 4
…ce Classification: Class II Review Panel: Gastroenterology/Urology Predicate Device: Occluder™ Occlusion Balloon Catheter (K133750) Device Description: The UPJ Occlusion Balloon Catheter is composed of a balloon catheter, a removable inflation/injection adapt…
Boston Scientific Corporation2014—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 35 years and passes through 3 companies; a new generation was cleared every 29.4 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All EYB devices

EYB Catheter, Ureteral, Gastro-Urology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · EYB

1in 2020

2009: 12010: 12014: 12017: 12018: 22019: 32020: 1
2007high 3 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EYB

248in 2019

2019: 248 days median
2007high 248 (2019)2026

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

Recalls per year · EYB

2so far in 2026, the most since 2007

2008: 12022: 12026 (partial year): 2
2007high 2 (2026) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EYB

11in 2025

2007: 142008: 152009: 422010: 132011: 112012: 102013: 142014: 92015: 92016: 42017: 102018: 82019: 222020: 132021: 112022: 52023: 232024: 122025: 11
2007high 42 (2009) · low 4 (2016)2025

MAUDE reports naming product code EYB, 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—014
20080—115
20091—042
20101—013
20110—011
20120—010
20130—014
20141—09
20150—09
20160—04
20171—010
20182—08
20193248022
20201—013
20210—011
20220—15
20230—023
20240—012
20250—011
20260—2—

What is it indicated for?

Used to temporarily occlude the ureteropelvic junction to prevent stone fragments from entering the ureter during percutaneous lithotripsy, and for injection of contrast medium.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K183323: UPJ Occlusion Balloon Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K183323

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026