510(k) Report

510(k) · Cleared

Cleared

Catco Urological Catheter

K944782510(k) TraditionalCleared Oct 13, 199416-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

Catco Medical, Inc. · EZD Catheter, Straight

Cleared on Oct 13, 1994 after a 16-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
Oct 13, 1994
Review
16 days
Class
Class II
Product code
EZD
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2007: 1 descendant cleared2020: 1 descendant cleared1990200020102020
  1. This deviceK944782 Catco Urological CatheterCatco Medical, Inc. · 1994
  2. Descendant · cites it directly · 1 of its ownK072997 Neomed Urinary CatheterNeomed, Inc. · 2007
  3. Descendant · 2 generations on · 0 of its ownK202566 Wiygul CatheterBig Blue Biotech, Inc. · 2020

Most influential descendants

Showing 2 of 2 · See all
  • K072997Neomed Urinary CatheterNeomed, Inc. · 2007 · cites it directly1descendant
  • K202566Wiygul CatheterBig Blue Biotech, Inc. · 2020 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K944782Catco Urological CatheterCatco Medical, Inc.1994—
+1K072997Neomed Urinary CatheterNeomed, Inc.2007—
+2K202566Wiygul CatheterBig Blue Biotech, Inc.2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
202010
FIG. 1 — Lineage of K944782, 1994–2020Source: 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 EZD? 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 EZD device

  1. #1 K241210 Luja Coudescore 16.2 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K072997Neomed Urinary CatheterNeomed, Inc.20071

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, K072997 (Neomed, Inc., 2007) has gone furthest, with 1 descendant of its own.

How does its category compare?

All EZD devices

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

FDA decisions per year · EZD

11so far in 2026, the most since 2007

2007: 42008: 12009: 22010: 22011: 42012: 22013: 42014: 52015: 12016: 32017: 22018: 32020: 12022: 102023: 62024: 52025: 62026 (partial year): 11
2007high 11 (2026) · low 0 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EZD

130in 2025

2007: 121 days median2011: 116 days median2013: 110 days median2014: 91 days median2016: 83 days median2018: 122 days median2022: 288 days median2023: 214 days median2024: 147 days median2025: 130 days median2026 (partial year): 146 days median
2007high 288 (2022) · low 83 (2016)2026

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

Recalls per year · EZD

1in 2014

2011: 12012: 12014: 1
2007high 1 (2011) · low 0 (2007)2026

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

Adverse event reports per year · EZD

288in 2025

2009: 42010: 62011: 42012: 22013: 182014: 172015: 212016: 212017: 1202018: 3902019: 4662020: 5632021: 9942022: 4872023: 5532024: 1162025: 288
2007high 994 (2021) · low 0 (2007)2025

MAUDE reports naming product code EZD, 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
2007412100
20081—00
20092—04
20102—06
2011411614
20122—12
20134110018
2014591117
20151—021
2016383021
20172—0120
201831220390
20190—0466
20201—0563
20210—0994
2022102880487
202362140553
202451470116
202561300288
2026111460—
Cite this page

510(k) Report. “K944782: Catco Urological Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K944782

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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