510(k) Report

510(k) · Cleared

Cleared

Pentax Medical Valve Set

K222980510(k) TraditionalCleared Nov 21, 202254-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

Yangzhou Fartley Medical Instrument Technology Co., Ltd. · ODC Endoscope Channel Accessory

Cleared on Nov 21, 2022 as substantially equivalent to K220210 (Yangzhou Fartley Medical Instrument Technology Co., Ltd., 2022) after a 54-day review. Its family tree reaches back 5 generations to 1988.

Decided
Nov 21, 2022
Review
54 days
Class
Class II
Product code
ODC
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K884836 (1988). 11 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK884836 Universal Generator Irrigator Model Ugi-3000Meditron Devices, Inc. · 1988
  2. 4 generations backK031773 Endo Gator SystemByrne Medical, Inc. · 2003
  3. 3 generations backK092429 EndogatorByrne Medical, Inc. · 2009
  4. 2 generations backK200769 Disposable Endoscope Valves Set, Disposable Endoscope Valves Set BWilson Instruments (Sha) Co., Ltd. · 2021
  5. 1 generation backK220210 Disposable Endoscopy Adapter SetYangzhou Fartley Medical Instrument Technology Co., Ltd. · 2022
  6. This deviceK222980 Pentax Medical Valve SetYangzhou Fartley Medical Instrument Technology Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K884836Universal Generator Irrigator Model Ugi-3000Meditron Devices, Inc.1988—
−4K031773Endo Gator SystemByrne Medical, Inc.2003—
−3K092429EndogatorByrne Medical, Inc.2009—
−2K200769Disposable Endoscope Valves Set, Disposable Endoscope Valves Set BWilson Instruments (Sha) Co., Ltd.2021—
−1K220210Disposable Endoscopy Adapter SetYangzhou Fartley Medical Instrument Technology Co., Ltd.2022—
0 (this device)K222980Pentax Medical Valve SetYangzhou Fartley Medical Instrument Technology Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200020
200910
201020
FIG. 1 — Lineage of K222980, 1988–2022Source: 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 14.1 · 6 generations · 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? (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
*K220210Disposable Endoscopy Adapter Set
Summary page 4
…Endoscope and Accessories Product Code: ODC 5.3 Predicate Device Device Name: Disposable Endoscopy Adapter Set, K220210 Manufacturer: Yangzhou Fartley Medical Instrument Technology Co., Ltd. Classification Name: En…
Yangzhou Fartley Medical Instrument Technology Co., Ltd.2022—

Also cleared against K220210: 2 other devices →

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 34 years and passes through 4 companies; a new generation was cleared every 6.4 years on median.
  • 2 of the 11 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K220210.

How does its category compare?

All ODC devices

ODC Endoscope Channel Accessory: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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 Pentax Medical Valve Set is a collection of several sterile units. It is intended to be fitted to Pentax endoscopes’ working channels/ports to control the flow of fluids, gases and other materials. - Disposable Air/Water Valve: This unit is intended to be fitted to an endoscope air/water channel to control the inflow of medical gases and water, whilst preventing back-flow. - Disposable Suction Valve: This unit is intended to be fitted to an endoscope…

Read the full statement (144 words)

The Pentax Medical Valve Set is a collection of several sterile units. It is intended to be fitted to Pentax endoscopes’ working channels/ports to control the flow of fluids, gases and other materials.

- Disposable Air/Water Valve: This unit is intended to be fitted to an endoscope air/water channel to control the inflow of medical gases and water, whilst preventing back-flow.

- Disposable Suction Valve: This unit is intended to be fitted to an endoscope suction channel to control the operations of suction, whilst preventing inflow of air.

- Disposable Biopsy Valve: This unit is intended to be fitted to an endoscope biopsy port to prevent leakage of gases and body fluids during an endoscopic procedure.

- Disposable Water Jet Adapter: This unit 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. “K222980: Pentax Medical Valve Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222980

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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