510(k) Report

510(k) · Cleared

Cleared

Rutner Universal Wedge Catheter

K760858510(k) TraditionalCleared Dec 6, 197649-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, Inc. · KOD Catheter, Urological

Cleared on Dec 6, 1976 after a 49-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Dec 6, 1976
Review
49 days
Class
Class II
Product code
KOD
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2018: 1 descendant cleared19801990200020102020
  1. This deviceK760858 Rutner Universal Wedge CatheterCook, Inc. · 1976
  2. Descendant · cites it directly · 0 of its ownK171810 Cone Tip Ureteral Catheter, Rutner Universal Wedge CatheterCook Incorporated · 2018

Most influential descendants

Showing 1 of 1 · See all
  • K171810Cone Tip Ureteral Catheter, Rutner Universal Wedge CatheterCook Incorporated · 2018 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K760858Rutner Universal Wedge CatheterCook, Inc.1976—
+1K171810Cone Tip Ureteral Catheter, Rutner Universal Wedge CatheterCook Incorporated2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
FIG. 1 — Lineage of K760858, 1976–2018Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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

Planning a device in KOD? 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 KOD device

  1. #1 K251864 Rubber Utility Catheterscore 10.9 · 1 generation · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K171810Cone Tip Ureteral Catheter, Rutner Universal Wedge CatheterCook Incorporated20180

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?

  • Of its descendants, K171810 (Cook Incorporated, 2018) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KOD devices

KOD Catheter, Urological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KOD

2in 2022

2008: 22009: 12010: 12011: 22014: 12016: 22017: 12018: 62019: 12021: 12022: 22026 (partial year): 1
2007high 6 (2018) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KOD

251in 2018

2018: 251 days median
2007high 251 (2018)2026

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

Recalls per year · KOD

1in 2023

2009: 152010: 12011: 472012: 22016: 12019: 12022: 32023: 1, 1 Class I2026 (partial year): 1
2007high 47 (2011) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · KOD

1,389in 2025

2007: 1802008: 1022009: 1832010: 2282011: 2092012: 1652013: 3932014: 2262015: 4182016: 2842017: 1,8732018: 1,1792019: 1,1672020: 1,3702021: 1,3882022: 1,2802023: 1,1602024: 1,2592025: 1,389
2007high 1,873 (2017) · low 102 (2008)2025

MAUDE reports naming product code KOD, 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—0180
20082—0102
20091—15183
20101—1228
20112—47209
20120—2165
20130—0393
20141—0226
20150—0418
20162—1284
20171—01,873
2018625101,179
20191—11,167
20200—01,370
20211—01,388
20222—31,280
20230—1 (1)1,160
20240—01,259
20250—01,389
20261—1—
Cite this page

510(k) Report. “K760858: Rutner Universal Wedge Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K760858

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026