510(k) Report

510(k) · Cleared

Cleared

FUJIFILM Distal Cap Models 33-40

K193123510(k) SpecialCleared Dec 11, 201929-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 Dec 11, 2019 as substantially equivalent to K162749 (Fujifilm Medical Systems U.S.A, Inc., 2017) after a 29-day review. Its family tree reaches back 5 generations to 2000. 2 later devices descend from it.

Decided
Dec 11, 2019
Review
29 days
Class
Class II
Product code
FDS
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K993704 (2000). 8 ancestors in all, the oldest K944759 (1995). 2 later devices descend from it, 2 citing it directly.

  1. Root · 5 generations backK993704 Gastro-Intestinal System EN-410WMFujinon, Inc. · 2000
  2. 4 generations backK040048 Fujinon Double Balloon Enteroscopy SystemFujinon, Inc. · 2004
  3. 3 generations backK090116 Fujinon Colonoscope for Double Balloon Enterscopy System Model…Fujinon, Inc. · 2009
  4. 2 generations backK143556 Fujifilm Double Balloon Endoscopes Models EN-530T and EN-580TFujifilm Medical Systems U.S.A, Inc. · 2015
  5. 1 generation backK162749 FUJIFILM Hood Models DH-28GR, DH-29CR and DH-30CRFujifilm Medical Systems U.S.A, Inc. · 2017
  6. This deviceK193123 FUJIFILM Distal Cap Models 33-40Fujifilm Corporation · 2019
  7. Descendant · cites it directly · 0 of its ownK253568 Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood…Fujifilm Corporation · 2026
  8. Descendant · cites it directly · 0 of its ownK212296 Distal Cap Model DH-32EN, Distal Cap Model DH-17EN2Fujifilm Corporation · 2021

Most influential descendants

Showing 2 of 2 · See all
  • K253568Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood…Fujifilm Corporation · 2026 · cites it directly0descendants
  • K212296Distal Cap Model DH-32EN, Distal Cap Model DH-17EN2Fujifilm Corporation · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K993704Gastro-Intestinal System EN-410WMFujinon, Inc.2000—
−4K040048Fujinon Double Balloon Enteroscopy SystemFujinon, Inc.2004—
−3K090116Fujinon Colonoscope for Double Balloon Enterscopy System Model, EC-450B15Fujinon, Inc.2009—
−2K143556Fujifilm Double Balloon Endoscopes Models EN-530T and EN-580TFujifilm Medical Systems U.S.A, Inc.2015—
−1K162749FUJIFILM Hood Models DH-28GR, DH-29CR and DH-30CRFujifilm Medical Systems U.S.A, Inc.2017—
0 (this device)K193123FUJIFILM Distal Cap Models 33-40Fujifilm Corporation2019—
+1K253568Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood…Fujifilm Corporation2026—
+1K212296Distal Cap Model DH-32EN, Distal Cap Model DH-17EN2Fujifilm Corporation2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199520
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202610
FIG. 1 — Lineage of K193123, 2000–2026Source: 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? (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
*K162749FUJIFILM Hood Models DH-28GR, DH-29CR and DH-30CR
Summary page 4
…Endoscope and accessories, 21 C.F.R. § 876.1500 Product Codes: FDS, FDF Predicate Device: FUJIFILM Hood Models DH-28GR, DH-29CR, DH-30CR (K162749) Intended Use / Indications for Use: Distal Cap Models DH-33GR, DH-34CR, and DH-40GR are intended to be used in combination wit…
Fujifilm Medical Systems U.S.A, Inc.2017—

Also cleared against K162749: 4 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K253568Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood…Fujifilm Corporation20260
K212296Distal Cap Model DH-32EN, Distal Cap Model DH-17EN2Fujifilm Corporation20210

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 19 years and passes through 3 companies; a new generation was cleared every 4.3 years on median.
  • 3 of the 8 ancestors have a recall of any class.
  • Of its descendants, K253568 (Fujifilm Corporation, 2026) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K162749.

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. 2019, 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?

Distal Cap Models DH-33GR, DH-34CR, and DH-40GR are intended to be used in combination with compatible endoscopes to maintain the field of view during endoscopic procedures such as mucosal resection.

Distal Cap Models DH-35GZ, DH-37CZ, DH-38CZ, and DH-39CZ are intended to be used in combination with compatible endoscopes to maintain the field of view during observation of the digestive tract.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K193123: FUJIFILM Distal Cap Models 33-40.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K193123

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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