510(k) Report

510(k) · Cleared

Cleared

Water Bottle Cap Irrigaton System

K120862510(k) TraditionalCleared Nov 27, 2012250-day reviewClass II21 CFR 876.1500

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

Endochoice, Inc. · FEQ Pump, Air, Non-Manual, For Endoscope

Cleared on Nov 27, 2012 as substantially equivalent to K092429 (Byrne Medical, Inc., 2009) after a 250-day review. Its family tree reaches back 3 generations to 1988. 3 later devices descend from it.

Decided
Nov 27, 2012
Review
250 days
Class
Class II
Product code
FEQ
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K884836 (1988). 5 ancestors in all. 3 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1997: 1 other ancestor2014: 1 descendant cleared2016: 1 descendant cleared2019: 1 descendant clearedK884836 · Universal Generator Irrigator Model Ugi-3000 · Meditron Devices, Inc. · 1988K031773 · Endo Gator System · Byrne Medical, Inc. · 2003K092429 · Endogator · Byrne Medical, Inc. · 20091990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 1 descendant K092429 · Endogator · Byrne Medical, Inc. · 2009K031773 · Endo Gator System · Byrne Medical, Inc. · 2003K884836 · Universal Generator Irrigator Model Ugi-3000 · Meditron Devices, Inc. · 19880
  1. Root · 3 generations backK884836 Universal Generator Irrigator Model Ugi-3000Meditron Devices, Inc. · 1988
  2. 2 generations backK031773 Endo Gator SystemByrne Medical, Inc. · 2003
  3. 1 generation backK092429 EndogatorByrne Medical, Inc. · 2009
  4. This deviceK120862 Water Bottle Cap Irrigaton SystemEndochoice, Inc. · 2012
  5. Descendant · cites it directly · 2 of its ownK133747 Endochoice Water Bottle Cap Irrigation SystemEndochoice, Inc. · 2014
  6. Descendant · 2 generations on · 1 of its ownK161482 EndoChoice Water Bottle Cap Irrigation SystemEndochoice, Inc. · 2016
  7. Descendant · 3 generations on · 0 of its ownK181457 EndoStream (TM)Partnership Medical Limited · 2019

Most influential descendants

Showing 3 of 3 · See all
  • K133747Endochoice Water Bottle Cap Irrigation SystemEndochoice, Inc. · 2014 · cites it directly2descendants
  • K161482EndoChoice Water Bottle Cap Irrigation SystemEndochoice, Inc. · 2016 · 2 generations on1descendant
  • K181457EndoStream (TM)Partnership Medical Limited · 2019 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K884836Universal Generator Irrigator Model Ugi-3000Meditron Devices, Inc.1988—
−2K031773Endo Gator SystemByrne Medical, Inc.2003—
−1K092429EndogatorByrne Medical, Inc.2009—
0 (this device)K120862Water Bottle Cap Irrigaton SystemEndochoice, Inc.2012—
+1K133747Endochoice Water Bottle Cap Irrigation SystemEndochoice, Inc.2014—
+2K161482EndoChoice Water Bottle Cap Irrigation SystemEndochoice, Inc.2016—
+3K181457EndoStream (TM)Partnership Medical Limited2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201610
201910
FIG. 1 — Lineage of K120862, 1988–2019Source: 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), 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 FEQ? 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 FEQ device

  1. #1 K220395 EndoGator Endoscopy Irrigation Tubingscore 15.6 · 3 generations · no Class I recall
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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
*K092429Endogator
Summary page 1
…ame: Water bottle cap irrigation system Classification Name: FEQ; Endoscope and accessories Predicate Device(s): Byrne Medica, Inc. Endoator System (K(092429) General Device The Endohoice water bottle cap irrigation system is Description: designed to supply s…
Byrne Medical, Inc.2009—

Also cleared against K092429: 12 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K133747Endochoice Water Bottle Cap Irrigation SystemEndochoice, Inc.20142

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 24 years and passes through 3 companies; a new generation was cleared every 6.4 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K133747 (Endochoice, Inc., 2014) has gone furthest, with 2 descendants of its own.
  • 12 other devices also cite its predicate K092429.

How does its category compare?

All FEQ devices

FEQ Pump, Air, Non-Manual, For Endoscope: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · FEQ

1in 2022

2009: 12010: 32011: 12012: 32013: 12014: 12015: 22016: 32017: 12018: 22019: 12022: 1
2007high 3 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FEQ

29in 2016

2010: 84 days median2012: 141 days median2016: 29 days median
2007high 141 (2012) · low 29 (2016)2026

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

Recalls per year · FEQ

1in 2024

2011: 12013: 12015: 12024: 12026 (partial year): 1
2007high 1 (2011) · low 0 (2007)2026

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

Adverse event reports per year · FEQ

341in 2025

2008: 12009: 12011: 12012: 22013: 42015: 12016: 12017: 42018: 222019: 62020: 52021: 32022: 192023: 112024: 7052025: 341
2007high 705 (2024) · low 0 (2007)2025

MAUDE reports naming product code FEQ, 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—00
20080—01
20091—01
201038400
20111—11
2012314102
20131—14
20141—00
20152—11
201632901
20171—04
20182—022
20191—06
20200—05
20210—03
20221—019
20230—011
20240—1705
20250—0341
20260—1—

What is it indicated for?

The Water Bottle Cap irrigation system (tubing and accessories to accommodate various endoscopes; and irrigation pumps) is intended to provide irrigation via sterile water supply during GI endoscopic procedures when used in conjunction with an irrigation pump.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120862: Water Bottle Cap Irrigaton System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K120862

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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