510(k) Report

510(k) · Cleared

Cleared

EG-3630UR, Ultrasund Video Gastroscope

K013640510(k) TraditionalCleared Feb 4, 200291-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

Pentax Precision Instrument Corp. · FDS Gastroscope And Accessories, Flexible/Rigid

Cleared on Feb 4, 2002 as substantially equivalent to K961974 (Pentax Precision Instrument Corp., 1997) and 4 other predicates after a 91-day review. Its family tree reaches back 3 generations to 1982. 1 of the 24 devices in its family, counting itself, has a Class I recall. 9 later devices descend from it.

Decided
Feb 4, 2002
Review
91 days
Class
Class II
Product code
FDS
Recalls
None
Predicates
5

Its longest line of descent runs back 3 generations to K822846 (1982). 14 ancestors in all, the oldest K812810 (1981). 9 later devices descend from it, 1 citing it directly. 1 of the 24 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1998: 1 other ancestor1997: 2 other ancestors1994: 2 other ancestors1995: 1 other ancestor1992: 1 other ancestor1991: 1 other ancestor1985: 1 other ancestor, 1 with a Class I recall11981: 1 other ancestor2007: 1 descendant cleared2012: 1 descendant cleared2011: 1 descendant cleared2016: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant cleared2019: 1 descendant cleared2022: 2 descendants clearedK822846 · Pentax FC-38LA & FC-38SA Colonofiber · Pentax Precision Instrument Corp. · 1982×2: 2 generations cleared close together, K951574 (1996), K961564 (1996) 19801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 4 other ancestors2 generations back: 6 other ancestors, 1 with a Class I recall13 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 2 descendants4 generations forward: 2 descendants5 generations forward: 2 descendants K961564 · EG-2940, Video Gastroscope · Pentax Precision Instrument Corp. · 1996 · recalledK951574 · EC-3800L, Video Colonoscope · Pentax Precision Instrument Corp. · 1996 · recalledK822846 · Pentax FC-38LA & FC-38SA Colonofiber · Pentax Precision Instrument Corp. · 19820+5
  1. Root · 3 generations backK822846 Pentax FC-38LA & FC-38SA ColonofiberPentax Precision Instrument Corp. · 1982
  2. 2 generations backK951574 EC-3800L, Video ColonoscopePentax Precision Instrument Corp. · 1996 · Recalled
  3. 1 generation backK961564 EG-2940, Video GastroscopePentax Precision Instrument Corp. · 1996 · Recalled
  4. This deviceK013640 EG-3630UR, Ultrasund Video GastroscopePentax Precision Instrument Corp. · 2002
  5. Descendant · cites it directly · 8 of its ownK063847 Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR…Fujinon, Inc. · 2007 · Recalled
  6. Descendant · 2 generations on · 7 of its ownK111243 Fujinon Ultrasonic ProcessorFujinon, Inc. · 2011
  7. Descendant · 2 generations on · 4 of its ownK120446 Fujinon/Fujifilm Ultrasonic Endoscope EG-530UR2 and EG-530UT2Fujinon, Inc. · 2012 · Recalled
  8. Descendant · 3 generations on · 3 of its ownK181763 FUJIFILM Ultrasonic EndoscopeFujifilm Corporation · 2018
  9. Descendant · 4 generations on · 2 of its ownK183433 FUJIFILM Ultrasonic EndoscopeFujifilm Corporation · 2019

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2007: 12011: 12012: 12016: 12018: 12019: 12020: 12022: 2
2007high 2 (2022) · low 0 (2008)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 9 · See all
  • K063847Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR, EG-530UT and SU-700Fujinon, Inc. · 2007 · cites it directly8descendants
  • K111243Fujinon Ultrasonic ProcessorFujinon, Inc. · 2011 · 2 generations on7descendants
  • K120446Fujinon/Fujifilm Ultrasonic Endoscope EG-530UR2 and EG-530UT2Fujinon, Inc. · 2012 · 2 generations on4descendants
  • K181763FUJIFILM Ultrasonic EndoscopeFujifilm Corporation · 2018 · 3 generations on3descendants
  • K183433FUJIFILM Ultrasonic EndoscopeFujifilm Corporation · 2019 · 4 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K822846Pentax FC-38LA & FC-38SA ColonofiberPentax Precision Instrument Corp.1982—
−2K951574EC-3800L, Video ColonoscopePentax Precision Instrument Corp.19963
−1K961564EG-2940, Video GastroscopePentax Precision Instrument Corp.19962
0 (this device)K013640EG-3630UR, Ultrasund Video GastroscopePentax Precision Instrument Corp.2002—
+1K063847Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR, EG-530UT and SU-700Fujinon, Inc.20071
+2K111243Fujinon Ultrasonic ProcessorFujinon, Inc.2011—
+2K120446Fujinon/Fujifilm Ultrasonic Endoscope EG-530UR2 and EG-530UT2Fujinon, Inc.20121
+3K181763FUJIFILM Ultrasonic EndoscopeFujifilm Corporation2018—
+4K183433FUJIFILM Ultrasonic EndoscopeFujifilm Corporation2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198110
198511
199110
199210
199420
199510
199720
199810
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
201110
201210
201610
201810
201910
202010
202220
FIG. 1 — Lineage of K013640, 1982–2022Source: 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.

1 device in this family has a Class I recall. 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
Get a 510(k) Report

What was it cleared against? (5)

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
*K961974FG-36UX, Ultrasound Upper GI Fiberscope
Summary page 1
….1570}, Endoscope and Accessories (78KOG) {876.1500} Predicated Device(s) Information: Model, Description Manufacturer PMN# FG-36UX, Fiber Ultrasound Gastroscope PPIC K961974 EG-2940, Video Gastroscope PPIC K961564 EPM-3300, Video Processor PPIC K934918 EUB-525, Ultrasound Diagnostic Scanner Hitachi Ame…
Pentax Precision Instrument Corp.19972
*K961564EG-2940, Video Gastroscope
Summary page 1
…) {876.1500} Predicated Device(s) Information: Model, Description Manufacturer PMN# FG-36UX, Fiber Ultrasound Gastroscope PPIC K961974 EG-2940, Video Gastroscope PPIC K961564 EPM-3300, Video Processor PPIC K934918 EUB-525, Ultrasound Diagnostic Scanner Hitachi America K981434 EUB-6000, Ultrasound Diagno…
Pentax Precision Instrument Corp.19962
*K934918Epm-3300 Video Processor
Summary page 1
…rmation: Model, Description Manufacturer PMN# FG-36UX, Fiber Ultrasound Gastroscope PPIC K961974 EG-2940, Video Gastroscope PPIC K961564 EPM-3300, Video Processor PPIC K934918 EUB-525, Ultrasound Diagnostic Scanner Hitachi America K981434 EUB-6000, Ultrasound Diagnostic Scanner ' - Hitachi America K99402…
Pentax Precision Instrument Corp.1994—
*K981434Eup-OL334 Laparascopicprobe
Summary page 1
…Ultrasound Gastroscope PPIC K961974 EG-2940, Video Gastroscope PPIC K961564 EPM-3300, Video Processor PPIC K934918 EUB-525, Ultrasound Diagnostic Scanner Hitachi America K981434 EUB-6000, Ultrasound Diagnostic Scanner ' - Hitachi America K994026 Device Description: The EG-3630UR, Ultrasound Video Gastros…
Hitachi Medical Corp. of America1998—
*K994026Eub-6000 Ultrasound Diagnostic Scanner
Summary page 1
…K961564 EPM-3300, Video Processor PPIC K934918 EUB-525, Ultrasound Diagnostic Scanner Hitachi America K981434 EUB-6000, Ultrasound Diagnostic Scanner ' - Hitachi America K994026 Device Description: The EG-3630UR, Ultrasound Video Gastroscope, must be used with a Pentax Video Processor (software controlle…
Hitachi Medical Corp. of America2000—

Also cleared against K961974: 2 other devices →

What descends from it? (9)

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

NumberDeviceApplicantDecidedDescendants
K063847Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR, EG-530UT and SU-700Fujinon, Inc.20078

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K850020Pentax Pne- Ultra-Slim Upper G.I. Fiberscope FG-23Pentax Precision Instrument Corp. · 1985 · 2 generations back · ◆ in the 1985 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 20 years and passes through 1 company; a new generation was cleared every 5.6 years on median.
  • 4 of the 14 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K063847 (Fujinon, Inc., 2007) has gone furthest, with 8 descendants of its own.
  • 2 other devices also cite its predicate K961974.

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.

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?

The Ultrasound Video Gastroscope EG-3630UR is intended to provide ultrasonic and optical visualization of, and therapeutic access to, the Upper GI tract including esophagus, stomach, duodenum/small bowel in adult and pediatric patient populations.

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. “K013640: EG-3630UR, Ultrasund Video Gastroscope.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K013640

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026