510(k) Report

510(k) · Cleared

Cleared

FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP

K240142510(k) TraditionalCleared Sep 4, 2024230-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 · FDS Gastroscope And Accessories, Flexible/Rigid

Cleared on Sep 4, 2024 as substantially equivalent to K183572 (Fujifilm Corporation, 2019) and 3 other predicates after a 230-day review. Its family tree reaches back 7 generations to 1995. 3 later devices descend from it.

Decided
Sep 4, 2024
Review
230 days
Class
Class II
Product code
FDS
Recalls
None
Predicates
4

Its longest line of descent runs back 7 generations to K944759 (1995). 16 ancestors in all. 3 later devices descend from it, 2 citing it directly.

  1. Root · 7 generations backK944759 200 Series Gastro-Intestinal Video SystemFujinon, Inc. · 1995 · Recalled
  2. 6 generations backK041903 Fujinon G5 Colonoscopes, Models EC-450HL5 and EC-250HL5Fujinon, Inc. · 2004 · Recalled
  3. 5 generations backK112391 Fujinon ColonoscopesFujinon, Inc. · 2012
  4. 4 generations backK132210 Fujifilm 600 Series EndoscopesFujifilm Medical Systems U.S.A, Inc. · 2014
  5. 3 generations backK160196 Fujifilm Video Colonoscope Model EC-600WL V2Fujifilm Medical Systems U.S.A, Inc. · 2016
  6. 2 generations backK172916 FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and…Fujifilm Corporation · 2018
  7. 1 generation backK182836 FUJIFILM Endoscope Model EG-740NFujifilm Corporation · 2019
  8. This deviceK240142 FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T…Fujifilm Corporation · 2024
  9. Descendant · cites it directly · 1 of its ownK243260 FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860RFujifilm Corporation · 2025
  10. Descendant · 2 generations on · 0 of its ownK261880 FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy…Fujifilm Corporation · 2026
  11. Descendant · cites it directly · 0 of its ownK243512 FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T…Fujifilm Corporation · 2025

Most influential descendants

Showing 3 of 3 · See all
  • K243260FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860RFujifilm Corporation · 2025 · cites it directly1descendant
  • K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01Fujifilm Corporation · 2026 · 2 generations on0descendants
  • K243512FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope…Fujifilm Corporation · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K944759200 Series Gastro-Intestinal Video SystemFujinon, Inc.19955
−6K041903Fujinon G5 Colonoscopes, Models EC-450HL5 and EC-250HL5Fujinon, Inc.20041
−5K112391Fujinon ColonoscopesFujinon, Inc.2012—
−4K132210Fujifilm 600 Series EndoscopesFujifilm Medical Systems U.S.A, Inc.2014—
−3K160196Fujifilm Video Colonoscope Model EC-600WL V2Fujifilm Medical Systems U.S.A, Inc.2016—
−2K172916FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and…Fujifilm Corporation2018—
−1K182836FUJIFILM Endoscope Model EG-740NFujifilm Corporation2019—
0 (this device)K240142FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM…Fujifilm Corporation2024—
+1K243260FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860RFujifilm Corporation2025—
+2K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program…Fujifilm Corporation2026—
+1K243512FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM…Fujifilm Corporation2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
200010
200420
200710
200910
201510
201920

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202520
202610
FIG. 1 — Lineage of K240142, 1995–2026Source: 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 FDS? 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 FDS device

  1. #1 K251708 EvoEndo Single-Use Endoscopy Systemscore 16.5 · 12 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? (4)

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
*K183572FUJIFILM Endoscope Models EG-760CT, EC-760P-V/L and EC-740T/L
Summary page 5
…mber 876.1500 Product Code FDS | Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K183572 FUJIFILM Endoscope Model EG-760CT FDS K182836 FUJIFILM Endoscope Model EG-740N FDS K172916 FUJIFILM Endoscope Models EG-760R, EG-…
Fujifilm Corporation2019—
*K182836FUJIFILM Endoscope Model EG-740N
Summary page 5
…ted Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K183572 FUJIFILM Endoscope Model EG-760CT FDS K182836 FUJIFILM Endoscope Model EG-740N FDS K172916 FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/[g| | FDS K183032 FUJIFILM Dou…
Fujifilm Corporation2019—
*K172916FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/L and EC-760ZP-V/L, and FUJIFILM…
Summary page 5
…dicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K183572 FUJIFILM Endoscope Model EG-760CT FDS K182836 FUJIFILM Endoscope Model EG-740N FDS K172916 FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/[g| | FDS K183032 FUJIFILM Double Balloon Endoscope EI-580BT FDA Device Des…
Fujifilm Corporation2018—
*K183032FUJIFILM Double Balloon Endoscope EI580BT
Summary page 5
…t Code K183572 FUJIFILM Endoscope Model EG-760CT FDS K182836 FUJIFILM Endoscope Model EG-740N FDS K172916 FUJIFILM Endoscope Models EG-760R, EG-760Z, EC-760R-V/[g| | FDS K183032 FUJIFILM Double Balloon Endoscope EI-580BT FDA Device Description Summary 21 CFR 807.92(a)(4) A. Intended Use/indications for Us…
Fujifilm Corporation2019—

Also cleared against K183572: 1 other device →

What descends from it? (3)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K243260FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860RFujifilm Corporation20251
K243512FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope…Fujifilm Corporation20250

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 29 years and passes through 3 companies; a new generation was cleared every 2.1 years on median.
  • 3 of the 16 ancestors have a recall of any class.
  • Of its descendants, K243260 (Fujifilm Corporation, 2025) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K183572.

How does its category compare?

All FDS devices

FDS Gastroscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · FDS

8in 2025

2007: 22010: 12011: 12012: 32013: 22014: 22015: 22016: 12017: 12018: 62019: 52020: 22021: 52022: 22023: 32024: 52025: 82026 (partial year): 7
2007high 8 (2025) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FDS

211in 2025

2012: 181 days median2018: 167 days median2019: 175 days median2021: 78 days median2023: 133 days median2024: 220 days median2025: 211 days median2026 (partial year): 164 days median
2007high 220 (2024) · low 78 (2021)2026

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

Recalls per year · FDS

2in 2024

2013: 12016: 12020: 22024: 2
2007high 2 (2020) · low 0 (2007)2026

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

Adverse event reports per year · FDS

18,905in 2025

2007: 272008: 112009: 212010: 452011: 362012: 352013: 82014: 232015: 292016: 1082017: 1782018: 3042019: 1,3762020: 6012021: 1,7552022: 6,2162023: 9,8742024: 9,2582025: 18,905
2007high 18,905 (2025) · low 8 (2013)2025

MAUDE reports naming product code FDS, 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
20072—027
20080—011
20090—021
20101—045
20111—036
20123181035
20132—18
20142—023
20152—029
20161—1108
20171—0178
201861670304
2019517501,376
20202—2601
202157801,755
20222—06,216
2023313309,874
2024522029,258
20258211018,905
202671640—

What is it indicated for?

FUJIFILM Endoscope Models EG-840T and EG-840TP is intended for the visualization of the upper digestive tract, specifically for the observation, diagnosis, and endoscopic treatment of the esophagus, stomach, and duodenum.

FUJIFILM Endoscope Model EG-840N is intended for the visualization of the upper digestive tract, specifically for the observation, diagnosis, and endoscopic treatment of the esophagus, stomach, and duodenum. This product can be inserted orally or nasally.

Never use this product for any other purposes.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K240142: FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K240142

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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