510(k) Report

510(k) · Cleared

Cleared

EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)

K251859510(k) TraditionalCleared Oct 3, 2025108-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

Olympus Medical Systems Corporation · ODG Endoscopic Ultrasound System, Gastroenterology-Urology

Cleared on Oct 3, 2025 as substantially equivalent to K051541 (Olympus America, Inc., 2005) after a 108-day review. Its family tree reaches back 4 generations to 1986. 1 later device descends from it.

Decided
Oct 3, 2025
Review
108 days
Class
Class II
Product code
ODG
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K853585 (1986). 7 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK853585 Olympus Evs-Endoscopic Video Image & Data SysOlympus Corp. · 1986 · Recalled
  2. 3 generations backK954451 Evis 140 SystemOlympus America, Inc. · 1996 · Recalled
  3. 2 generations backK971660 Olympus GF-UM130 Ultrasound Gastrovideoscope, Its Associated…Olympus America, Inc. · 1997 · Recalled
  4. 1 generation backK051541 GF-UE160-AL5 Ultrasound EndoscopeOlympus America, Inc. · 2005 · Recalled
  5. This deviceK251859 EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation · 2025
  6. Descendant · cites it directly · 0 of its ownK261183 EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K853585Olympus Evs-Endoscopic Video Image & Data SysOlympus Corp.19862
−3K954451Evis 140 SystemOlympus America, Inc.19963
−2K971660Olympus GF-UM130 Ultrasound Gastrovideoscope, Its Associated Accessories and…Olympus America, Inc.19972
−1K051541GF-UE160-AL5 Ultrasound EndoscopeOlympus America, Inc.20052
0 (this device)K251859EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation2025—
+1K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199320
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K251859, 1986–2026Source: 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 ODG? 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 ODG device

  1. #1 K260428 RIVOS™ EUS Access Device (M00553900)score 13.0 · 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
*K051541GF-UE160-AL5 Ultrasound Endoscope
Summary page 5
…510(k) No. OLYMPUS GF-UE160-AL5 Endoscope used with OLYMPUS MEDICAL the Aloka SSD-5000 Diagnostic Ultrasound SYSTEMS CORP. K051541 System 510(k) Summary Page 1 of…
Olympus America, Inc.20052
†K112680Evis Exera Iii Video SystemOlympus Medical Systems Corporation20126

Also cleared against K051541: 2 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
K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)Olympus Medical Systems Corporation20260

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 39 years and passes through 3 companies; a new generation was cleared every 10.2 years on median.
  • 6 of the 7 ancestors have a recall of any class.
  • Of its descendants, K261183 (Olympus Medical Systems Corporation, 2026) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K051541.

How does its category compare?

All ODG devices

ODG Endoscopic Ultrasound System, Gastroenterology-Urology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · ODG

2in 2025

2009: 22011: 22013: 22014: 12016: 12017: 42018: 32019: 12020: 22021: 12022: 42023: 12024: 12025: 22026 (partial year): 2
2007high 4 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODG

71in 2022

2017: 75 days median2018: 30 days median2022: 71 days median
2007high 75 (2017) · low 30 (2018)2026

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

Recalls per year · ODG

4in 2020

2020: 42026 (partial year): 4
2007high 4 (2020) · low 0 (2007)2026

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

Adverse event reports per year · ODG

3,569in 2025

2008: 12009: 32010: 22011: 132012: 62013: 22014: 12015: 112016: 502017: 822018: 662019: 962020: 4452021: 1,2342022: 1,8322023: 2,0782024: 1,9042025: 3,569
2007high 3,569 (2025) · low 0 (2007)2025

MAUDE reports naming product code ODG, 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
20092—03
20100—02
20112—013
20120—06
20132—02
20141—01
20150—011
20161—050
2017475082
2018330066
20191—096
20202—4445
20211—01,234
202247101,832
20231—02,078
20241—01,904
20252—03,569
20262—4—

What is it indicated for?

The EVIS EUS ULTRASOUND GASTROINTESTINAL VIDEOSCOPE OLYMPUS GF-UE190 has been designed to be used with diagnostic ultrasound system, video system center, light source, documentation equipment, monitor, endoscopic therapy accessories and other ancillary equipment.

The EVIS EUS ULTRASOUND GASTROINTESTINAL VIDEOSCOPE OLYMPUS GF-UE190 is designed for endoscopic real-time ultrasound imaging, and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.

Operator qualifications

Appropriately trained healthcare professionals.

Device use settings

Healthcare facility

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K251859: EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K251859

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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