510(k) Report

510(k) · Cleared

Cleared

FUJIFILM Endoscope Model EC-760Z-V/L

K192664510(k) TraditionalCleared Nov 20, 201956-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

Fujifilm Corporation · FDF Colonoscope And Accessories, Flexible/Rigid

Cleared on Nov 20, 2019 as substantially equivalent to K172916 (Fujifilm Corporation, 2018) after a 56-day review. Its family tree reaches back 6 generations to 1995.

Decided
Nov 20, 2019
Review
56 days
Class
Class II
Product code
FDF
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K944759 (1995). 8 ancestors in all. No later device cites it as a predicate yet.

  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 deviceK192664 FUJIFILM Endoscope Model EC-760Z-V/LFujifilm Corporation · 2019
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)K192664FUJIFILM Endoscope Model EC-760Z-V/LFujifilm Corporation2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
200410
FIG. 1 — Lineage of K192664, 1995–2019Source: 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 FDF? 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 FDF device

  1. #1 K230332 Ambu® aScope™ Colon; Ambu® aBox™ 2score 20.1 · 8 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
*K172916FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and FUJIFILM…
Summary page 4
…ndoscope and accessories Regulation number: 21 C.F.R. 876.1500 Product Code: FDF Predicate Device: FUJIFILM Endoscope Model EC-760ZP-V/L (K172916) Reference Device: FUJIFILM Endoscope Model EC-760S-V/L (K190649) Intended Use / Indications for Use: EC-760Z-V/L is inten…
Fujifilm Corporation2018—
†K190649FUJIFILM Endoscope Model EC-760S-V/LFujifilm Corporation2019—

Also cleared against K172916: 10 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 24 years and passes through 3 companies; a new generation was cleared every 2.1 years on median.
  • 3 of the 8 ancestors have a recall of any class.
  • 10 other devices also cite its predicate K172916.

How does its category compare?

All FDF devices

FDF Colonoscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · FDF

4in 2025

2007: 42008: 22009: 62010: 42011: 22012: 72013: 22014: 62015: 22016: 72017: 42018: 72019: 42020: 42021: 32022: 52023: 62024: 22025: 42026 (partial year): 5
2007high 7 (2012) · low 2 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FDF

194in 2025

2007: 70 days median2009: 91 days median2010: 101 days median2012: 241 days median2014: 164 days median2016: 98 days median2017: 36 days median2018: 101 days median2019: 56 days median2020: 250 days median2021: 30 days median2022: 147 days median2023: 203 days median2025: 194 days median2026 (partial year): 147 days median
2007high 250 (2020) · low 30 (2021)2026

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

Recalls per year · FDF

8in 2023

2015: 12016: 12020: 12023: 8
2007high 8 (2023) · low 0 (2007)2026

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

Adverse event reports per year · FDF

17,231in 2025

2007: 812008: 682009: 832010: 482011: 772012: 882013: 632014: 602015: 1002016: 1702017: 3702018: 3882019: 4172020: 6872021: 2,4442022: 8,3452023: 11,7482024: 12,1282025: 17,231
2007high 17,231 (2025) · low 48 (2010)2025

MAUDE reports naming product code FDF, 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
2007470081
20082—068
2009691083
20104101048
20112—077
20127241088
20132—063
20146164060
20152—1100
20167981170
20174360370
201871010388
20194560417
202042501687
202133002,444
2022514708,345
20236203811,748
20242—012,128
20254194017,231
202651470—

What is it indicated for?

EC-760Z-V/L is intended for the visualization of the lower digestive tract, specifically for the observation, diagnosis, and endoscopic treatment of the rectum and large intestine.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192664: FUJIFILM Endoscope Model EC-760Z-V/L.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192664

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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