510(k) Report

510(k) · Cleared

Cleared

Seal Single-Use Biopsy Valve

K133734510(k) SpecialCleared Mar 19, 2014100-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. · OCX Endoscopic Irrigation/Suction System

Cleared on Mar 19, 2014 as substantially equivalent to K111821 (Endochoice, Inc., 2011) after a 100-day review. Its family tree reaches back 1 generation to 2011. 4 later devices descend from it.

Decided
Mar 19, 2014
Review
100 days
Class
Class II
Product code
OCX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K111821 (2011). 4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2016: 1 descendant cleared2018: 2 descendants cleared2025: 1 descendant clearedK111821 · Biopsy Valve · Endochoice, Inc. · 20112010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 1 descendant K111821 · Biopsy Valve · Endochoice, Inc. · 20110
  1. Root · 1 generation backK111821 Biopsy ValveEndochoice, Inc. · 2011
  2. This deviceK133734 Seal Single-Use Biopsy ValveEndochoice, Inc. · 2014
  3. Descendant · cites it directly · 3 of its ownK161167 Seal Single-Use Biopsy ValveEndochoice, Inc. · 2016
  4. Descendant · 2 generations on · 1 of its ownK182275 Seal Single Use Biopsy ValveBoston Scientific Corporation · 2018
  5. Descendant · 3 generations on · 0 of its ownK251997 Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems Corporation · 2025
  6. Descendant · 2 generations on · 0 of its ownK173758 Disposable Biopsy ValveZhejiang Chuangxiang Medical Technology Co., Ltd. · 2018

Most influential descendants

Showing 4 of 4 · See all
  • K161167Seal Single-Use Biopsy ValveEndochoice, Inc. · 2016 · cites it directly3descendants
  • K182275Seal Single Use Biopsy ValveBoston Scientific Corporation · 2018 · 2 generations on1descendant
  • K251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems Corporation · 2025 · 3 generations on0descendants
  • K173758Disposable Biopsy ValveZhejiang Chuangxiang Medical Technology Co., Ltd. · 2018 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K111821Biopsy ValveEndochoice, Inc.2011—
0 (this device)K133734Seal Single-Use Biopsy ValveEndochoice, Inc.2014—
+1K161167Seal Single-Use Biopsy ValveEndochoice, Inc.2016—
+2K182275Seal Single Use Biopsy ValveBoston Scientific Corporation2018—
+3K251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems Corporation2025—
+2K173758Disposable Biopsy ValveZhejiang Chuangxiang Medical Technology Co., Ltd.2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201820
202510
FIG. 1 — Lineage of K133734, 2011–2025Source: 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 OCX? 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 OCX device

  1. #1 K251986 Auxiliary Water Tube Maj-855score 12.8 · 10 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
*K111821Biopsy Valve
Summary page 2
…low from the endloscope, and out of the biopsy valve. 7. Substantial Equivalence: The device submitted for review isa modification of the Biopsy Valve (K111821). Changes to the device include a modification in material, and a change in dimensions. Both the modified and unmodif…
Endochoice, Inc.2011—

Also cleared against K111821: 3 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K161167Seal Single-Use Biopsy ValveEndochoice, Inc.20163

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?

  • Its one ancestor has no recall.
  • Of its descendants, K161167 (Endochoice, Inc., 2016) has gone furthest, with 3 descendants of its own.
  • 3 other devices also cite its predicate K111821.

How does its category compare?

All OCX devices

OCX Endoscopic Irrigation/Suction System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · OCX

4in 2025

2009: 12010: 32011: 12012: 42013: 32014: 62015: 22016: 22018: 52019: 82020: 42021: 32022: 62023: 72024: 42025: 4
2007high 8 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OCX

178in 2025

2010: 51 days median2012: 256 days median2013: 106 days median2014: 77 days median2018: 60 days median2019: 133 days median2020: 88 days median2021: 233 days median2022: 84 days median2023: 109 days median2024: 74 days median2025: 178 days median
2007high 256 (2012) · low 51 (2010)2026

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

Recalls per year · OCX

2in 2022

2015: 12020: 112022: 22026 (partial year): 2
2007high 11 (2020) · low 0 (2007)2026

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

Adverse event reports per year · OCX

33in 2025

2008: 12012: 12013: 12014: 52015: 92016: 82017: 92018: 182019: 412020: 112021: 82022: 182023: 462024: 212025: 33
2007high 46 (2023) · low 0 (2007)2025

MAUDE reports naming product code OCX, 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—00
201035100
20111—00
2012425601
2013310601
201467705
20152—19
20162—08
20170—09
2018560018
20198133041
20204881111
2021323308
2022684218
20237109046
2024474021
20254178033
20260—2—

What is it indicated for?

The Single-Use Biopsy Valve provides access for endoscopic device passage and exchange, helps maintain sufflation, and minimizes leakage of biomnaterial from biopsy port throughout the endoscopic procedure, and provides access for irrigation.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K133734: Seal Single-Use Biopsy Valve.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133734

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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