510(k) Report

510(k) · Cleared

Cleared

Andorate Disposable Air/Water Valve, Andorate Disposable Suction Valve

K200495510(k) TraditionalCleared Jun 24, 2020117-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

Ga Health Company Limited · ODC Endoscope Channel Accessory

Cleared on Jun 24, 2020 as substantially equivalent to K172916 (Fujifilm Corporation, 2018) after a 117-day review. Its family tree reaches back 6 generations to 1995. 1 later device descends from it.

Decided
Jun 24, 2020
Review
117 days
Class
Class II
Product code
ODC
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K944759 (1995). 8 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 6 generations backK944759 200 Series Gastro-Intestinal Video SystemFujinon, Inc. · 1995 · Recalled
  2. 5 generations backK041903 Fujinon G5 Colonoscopes, Models EC-450HL5 and EC-250HL5Fujinon, Inc. · 2004 · Recalled
  3. 4 generations backK112391 Fujinon ColonoscopesFujinon, Inc. · 2012
  4. 3 generations backK132210 Fujifilm 600 Series EndoscopesFujifilm Medical Systems U.S.A, Inc. · 2014
  5. 2 generations backK160196 Fujifilm Video Colonoscope Model EC-600WL V2Fujifilm Medical Systems U.S.A, Inc. · 2016
  6. 1 generation backK172916 FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and…Fujifilm Corporation · 2018
  7. This deviceK200495 Andorate Disposable Air/Water Valve, Andorate Disposable Suction ValveGa Health Company Limited · 2020
  8. Descendant · cites it directly · 0 of its ownK232118 ANDORATE® Valve KitGa Health Company Limited · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K232118ANDORATE® Valve KitGa Health Company Limited · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K944759200 Series Gastro-Intestinal Video SystemFujinon, Inc.19955
−5K041903Fujinon G5 Colonoscopes, Models EC-450HL5 and EC-250HL5Fujinon, Inc.20041
−4K112391Fujinon ColonoscopesFujinon, Inc.2012—
−3K132210Fujifilm 600 Series EndoscopesFujifilm Medical Systems U.S.A, Inc.2014—
−2K160196Fujifilm Video Colonoscope Model EC-600WL V2Fujifilm Medical Systems U.S.A, Inc.2016—
−1K172916FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and…Fujifilm Corporation2018—
0 (this device)K200495Andorate Disposable Air/Water Valve, Andorate Disposable Suction ValveGa Health Company Limited2020—
+1K232118ANDORATE® Valve KitGa Health Company Limited2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K200495, 1995–2023Source: 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 ODC? 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 ODC device

  1. #1 K232329 Defendo Fujifilm 700 Single Use Biopsy Valve…score 14.0 · 6 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? (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
*K172916FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and FUJIFILM…
Summary page 4
…ication: 2 Regulation Name: Endoscope and Accessories 5. Predicate Device Identification Predicate Device 510(k) No.: K172916 Predicate Device Trade Name: FUJIFILM Endoscope Predicate Device Product Code: ODC 6. Device Description:…
Fujifilm Corporation2018—

Also cleared against K172916: 10 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K232118ANDORATE® Valve KitGa Health Company Limited20230

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 25 years and passes through 4 companies; a new generation was cleared every 2.3 years on median.
  • 3 of the 8 ancestors have a recall of any class.
  • Of its descendants, K232118 (Ga Health Company Limited, 2023) has gone furthest, with 0 descendants of its own.
  • 10 other devices also cite its predicate K172916.

How does its category compare?

All ODC devices

ODC Endoscope Channel Accessory: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · ODC

6in 2025

2008: 32009: 12010: 42011: 42012: 22015: 22016: 12017: 12018: 22019: 42020: 42021: 62022: 82023: 72024: 82025: 62026 (partial year): 1
2007high 8 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODC

106in 2025

2008: 83 days median2010: 67 days median2011: 143 days median2019: 55 days median2020: 128 days median2021: 181 days median2022: 118 days median2023: 126 days median2024: 95 days median2025: 106 days median
2007high 181 (2021) · low 55 (2019)2026

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

Recalls per year · ODC

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

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

Adverse event reports per year · ODC

91in 2025

2012: 12013: 12014: 22015: 32016: 82017: 122018: 172019: 402020: 542021: 522022: 372023: 432024: 1002025: 91
2007high 100 (2024) · low 0 (2007)2025

MAUDE reports naming product code ODC, 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
200838300
20091—00
201046700
2011414300
20122—01
20130—01
20140—02
20152—03
20161—08
20171—012
20182—017
2019455040
20204128054
20216181052
20228118037
20237126043
20248950100
20256106091
20261—1—

What is it indicated for?

The Andorate® Disposable Suction Valve is used to control the suction function of an endoscope (Fujifilm 700 series) during a GI Endoscopic procedure.

The Andorate® Disposable Air/Water valve is used to control the air/water function of an endoscope (Fujifilm 700 series) during a GI Endoscopic procedure.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200495: Andorate Disposable Air/Water Valve, Andorate Disposable Suction Valve.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200495

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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