510(k) Report

510(k) · Cleared

Cleared

Video Laparoscope, Video Processor, Light Source

K192918510(k) TraditionalCleared Feb 20, 2020128-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 · GCJ Laparoscope, General & Plastic Surgery

Cleared on Feb 20, 2020 as substantially equivalent to K162836 (Fujifilm New Development U.S.A., Inc., 2017) and 1 other predicate after a 128-day review. Its family tree reaches back 11 generations to 1993. 3 of the 44 devices in its family, counting itself, have a Class I recall. 6 later devices descend from it.

Decided
Feb 20, 2020
Review
128 days
Class
Class II
Product code
GCJ
Recalls
None
Predicates
2

Its longest line of descent runs back 11 generations to K931154 (1993). 37 ancestors in all, the oldest K843084 (1985). 6 later devices descend from it, 2 citing it directly. 3 of the 44 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2017: 1 other ancestor2014: 1 other ancestor1998: 1 other ancestor2011: 1 other ancestor2006: 1 other ancestor2005: 2 other ancestors2001: 1 other ancestor2000: 4 other ancestors1995: 3 other ancestors2003: 1 other ancestor, 1 with a Class I recall12002: 1 other ancestor1996: 1 other ancestor1991: 2 other ancestors, 1 with a Class I recall11986: 1 other ancestor1993: 1 other ancestor1992: 2 other ancestors1985: 2 other ancestors2020: 1 descendant cleared2021: 2 descendants cleared2024: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant clearedReference device: K180414 · EPX-4440FN Digital Video Processor with Light Source · Fujifilm New Development U.S.A., Inc. · 2018Reference device: K182836 · FUJIFILM Endoscope Model EG-740N · Fujifilm Corporation · 2019Reference device: K983561 · Fujinon Evl-F Video Laproscope · Fujinon, Inc. · 1998K931154 · Evis 200 System · Olympus Corp. · 1993K963033 · BF 240/P240/IT240 Bronchovideoscope & Accessories · Olympus America, Inc. · 1996 · recalledK981543 · Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and Ancillary Equipment · The Olympus Optical Co. · 1998 · recalled×2: 2 generations cleared close together, K013591 (2001), K021073 (2002) K031648 · Visera Rhino-Laryngovideoscope Olympus Enf Type V · Olympus Optical Co., Ltd. · 2003K061313 · Evis Exera 180 System · Olympus Medical Systems Corporation · 2006 · Class I recallK100584 · Evis Exeraii 180 System · Olympus Medical Systems Corporation · 2010 · recalledK112680 · Evis Exera Iii Video System · Olympus Medical Systems Corporation · 2012 · recalledK122831 · Video System Center · Olympus Medical Systems Corp. · 2012K163675 · Processor VP-7000, Light Source BL-7000 · Fujifilm Medical System U.S.A., Inc. · 20171990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 1 other ancestor4 generations back: 5 other ancestors5 generations back: 6 other ancestors, 1 with a Class I recall16 generations back: 4 other ancestors, 1 with a Class I recall17 generations back: 7 other ancestors 1 generation forward: 2 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant K163675 · Processor VP-7000, Light Source BL-7000 · Fujifilm Medical System U.S.A., Inc. · 2017K122831 · Video System Center · Olympus Medical Systems Corp. · 2012K112680 · Evis Exera Iii Video System · Olympus Medical Systems Corporation · 2012 · recalledK100584 · Evis Exeraii 180 System · Olympus Medical Systems Corporation · 2010 · recalledK061313 · Evis Exera 180 System · Olympus Medical Systems Corporation · 2006 · Class I recallK031648 · Visera Rhino-Laryngovideoscope Olympus Enf Type V · Olympus Optical Co., Ltd. · 2003K021073 · Visera Rhinlaryngovideoscope Olympus Enf Type V · Olympus America, Inc. · 2002K013591 · Xenf-TP Rhino-Laryngofiberscope, Its Acessories and Ancillary Equipment · Olympus Optical Co., Ltd. · 2001K981543 · Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and Ancillary Equipment · The Olympus Optical Co. · 1998 · recalledK963033 · BF 240/P240/IT240 Bronchovideoscope & Accessories · Olympus America, Inc. · 1996 · recalledK931154 · Evis 200 System · Olympus Corp. · 1993−10−50
  1. Root · 11 generations backK931154 Evis 200 SystemOlympus Corp. · 1993
  2. 7 generations between
  3. 3 generations backK112680 Evis Exera Iii Video SystemOlympus Medical Systems Corporation · 2012 · Recalled
  4. 2 generations backK122831 Video System CenterOlympus Medical Systems Corp. · 2012
  5. 1 generation backK163675 Processor VP-7000, Light Source BL-7000Fujifilm Medical System U.S.A., Inc. · 2017
  6. This deviceK192918 Video Laparoscope, Video Processor, Light SourceFujifilm Corporation · 2020
  7. Descendant · cites it directly · 3 of its ownK203717 Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0Fujifilm Corporaton · 2021
  8. Descendant · 2 generations on · 1 of its ownK250268 HyperSnap Surgical System (HSS)Hypervision Surgical · 2025
  9. Descendant · cites it directly · 1 of its ownK202130 FUJIFILM Video LaparoscopeFujifilm Corporation · 2020
  10. Descendant · 3 generations on · 0 of its ownK253984 Instrument Exit Point on Touch Surgery™ AideCovidien, LLC · 2026
  11. Descendant · 2 generations on · 0 of its ownK233225 SCHOELLY Oxygen Saturation Imaging (OSI) Camera System (Camera…Schoelly Fiberoptic GmbH · 2024
Show all 11 generations
  1. Root · 11 generations backK931154 Evis 200 SystemOlympus Corp. · 1993
  2. 10 generations backK963033 BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc. · 1996 · Recalled
  3. 9 generations backK981543 Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories…The Olympus Optical Co. · 1998 · Recalled
  4. 8 generations backK013591 Xenf-TP Rhino-Laryngofiberscope, Its Acessories and Ancillary…Olympus Optical Co., Ltd. · 2001
  5. 7 generations backK021073 Visera Rhinlaryngovideoscope Olympus Enf Type VOlympus America, Inc. · 2002
  6. 6 generations backK031648 Visera Rhino-Laryngovideoscope Olympus Enf Type VOlympus Optical Co., Ltd. · 2003
  7. 5 generations backK061313 Evis Exera 180 SystemOlympus Medical Systems Corporation · 2006 · Recalled (Class I)
  8. 4 generations backK100584 Evis Exeraii 180 SystemOlympus Medical Systems Corporation · 2010 · Recalled
  9. 3 generations backK112680 Evis Exera Iii Video SystemOlympus Medical Systems Corporation · 2012 · Recalled
  10. 2 generations backK122831 Video System CenterOlympus Medical Systems Corp. · 2012
  11. 1 generation backK163675 Processor VP-7000, Light Source BL-7000Fujifilm Medical System U.S.A., Inc. · 2017
  12. This deviceK192918 Video Laparoscope, Video Processor, Light SourceFujifilm Corporation · 2020

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2020: 12021: 22024: 12025: 12026: 1
2020high 2 (2021) · low 0 (2022)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 6 · See all
  • K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0Fujifilm Corporaton · 2021 · cites it directly3descendants
  • K250268HyperSnap Surgical System (HSS)Hypervision Surgical · 2025 · 2 generations on1descendant
  • K202130FUJIFILM Video LaparoscopeFujifilm Corporation · 2020 · cites it directly1descendant
  • K253984Instrument Exit Point on Touch Surgery™ AideCovidien, LLC · 2026 · 3 generations on0descendants
  • K233225SCHOELLY Oxygen Saturation Imaging (OSI) Camera System (Camera Control Unit, Camera Head…Schoelly Fiberoptic GmbH · 2024 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K931154Evis 200 SystemOlympus Corp.1993—
−10K963033BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc.19966
−9K981543Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and…The Olympus Optical Co.19985
−8K013591Xenf-TP Rhino-Laryngofiberscope, Its Acessories and Ancillary EquipmentOlympus Optical Co., Ltd.2001—
−7K021073Visera Rhinlaryngovideoscope Olympus Enf Type VOlympus America, Inc.2002—
−6K031648Visera Rhino-Laryngovideoscope Olympus Enf Type VOlympus Optical Co., Ltd.2003—
−5K061313Evis Exera 180 SystemOlympus Medical Systems Corporation2006Class I
−4K100584Evis Exeraii 180 SystemOlympus Medical Systems Corporation20109
−3K112680Evis Exera Iii Video SystemOlympus Medical Systems Corporation20126
−2K122831Video System CenterOlympus Medical Systems Corp.2012—
−1K163675Processor VP-7000, Light Source BL-7000Fujifilm Medical System U.S.A., Inc.2017—
0 (this device)K192918Video Laparoscope, Video Processor, Light SourceFujifilm Corporation2020—
+1K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0Fujifilm Corporaton2021—
+2K250268HyperSnap Surgical System (HSS)Hypervision Surgical2025—
+1K202130FUJIFILM Video LaparoscopeFujifilm Corporation2020—
+3K253984Instrument Exit Point on Touch Surgery™ AideCovidien, LLC2026—
+2K233225SCHOELLY Oxygen Saturation Imaging (OSI) Camera System (Camera Control Unit…Schoelly Fiberoptic GmbH2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198520
198610
199121
199220
199310
199530
199610
199810
200040
200110
200210
200311
200520
200610
201110
201410
201710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202120
202410
202510
202610
FIG. 1 — Lineage of K192918, 1993–2026Source: 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.

3 devices in this family have 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 GCJ device

  1. #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 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? (2)

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
*K162836FUJIFILM Surgical System
Summary page 4
…FR Section Product Codes Endoscope and accessories 21 CFR 876.1500 GCJ, FET, NTN, NWB, PEA Predicate Device: • EL-580FN Video Laparoscope (K162836) • FUJIFILM Video Processor VP-7000 and Light Source BL-7000 (K163675) Reference Device: • VP-4440FN Video Processo…
Fujifilm New Development U.S.A., Inc.2017—
*K163675Processor VP-7000, Light Source BL-7000
Summary page 4
…R 876.1500 GCJ, FET, NTN, NWB, PEA Predicate Device: • EL-580FN Video Laparoscope (K162836) • FUJIFILM Video Processor VP-7000 and Light Source BL-7000 (K163675) Reference Device: • VP-4440FN Video Processor and XL-4450FN Light Source (K180414) • FUJIFILM Endoscope Model EG-7…
Fujifilm Medical System U.S.A., Inc.2017—
†K180414EPX-4440FN Digital Video Processor with Light SourceFujifilm New Development U.S.A., Inc.2018—
†K182836FUJIFILM Endoscope Model EG-740NFujifilm Corporation2019—
†K983561Fujinon Evl-F Video LaproscopeFujinon, Inc.1998—

Also cleared against K162836: 1 other device →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0Fujifilm Corporaton20213
K202130FUJIFILM Video LaparoscopeFujifilm Corporation20201

Has anything in its family been recalled? (3 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.

  • K061313Evis Exera 180 SystemOlympus Medical Systems Corporation · 2006 · 4 generations back · ◆ on the line of descent in FIG. 16 Class I recalls
  • K023984Modification to Olympus Bronchoscopes BF-40 Series, BF-240 Series, and BF-160 SeriesThe Olympus Optical Co. · 2003 · 5 generations back · ◆ in the 2003 ancestors bar of FIG. 114 Class I recalls
  • K912120Urf-P2 Ureterorenofiberscope/CholedochofiberscopeOlympus Corp. · 1991 · 6 generations back · ◆ in the 1991 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 27 years and passes through 8 companies; a new generation was cleared every 2.8 years on median.
  • 18 of the 37 ancestors have a recall of any class; 3 have a Class I recall.
  • Of its descendants, K203717 (Fujifilm Corporaton, 2021) has gone furthest, with 3 descendants of its own.
  • 1 other device also cites its predicate K162836.

How does its category compare?

All GCJ devices

GCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · GCJ

21in 2025

2007: 182008: 192009: 212010: 242011: 152012: 172013: 152014: 192015: 262016: 272017: 202018: 212019: 152020: 282021: 182022: 202023: 312024: 292025: 212026 (partial year): 26
2007high 31 (2023) · low 15 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GCJ

108in 2025

2007: 42 days median2008: 73 days median2009: 85 days median2010: 122 days median2011: 113 days median2012: 88 days median2013: 93 days median2014: 90 days median2015: 76 days median2016: 99 days median2017: 77 days median2018: 88 days median2019: 60 days median2020: 61 days median2021: 116 days median2022: 103 days median2023: 109 days median2024: 90 days median2025: 108 days median2026 (partial year): 122 days median
2007high 122 (2010) · low 42 (2007)2026

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

Recalls per year · GCJ

5in 2025

2007: 122008: 162009: 62010: 302011: 92012: 12013: 7, 1 Class I2014: 22016: 52017: 12018: 12022: 12023: 12025: 52026 (partial year): 1
2007high 30 (2010) · low 0 (2015)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GCJ

5,860in 2025

2007: 1,6392008: 1,3192009: 1,9952010: 2,6572011: 2,1332012: 1,5262013: 1,5652014: 1,7142015: 1,7102016: 2,0802017: 3,4682018: 2,5622019: 2,5782020: 2,6182021: 3,4312022: 3,9452023: 6,0022024: 6,0472025: 5,860
2007high 6,047 (2024) · low 1,319 (2008)2025

MAUDE reports naming product code GCJ, 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
20071842121,639
20081973161,319
2009218561,995
201024122302,657
20111511392,133
2012178811,526
201315937 (1)1,565
2014199021,714
2015267601,710
2016279952,080
2017207713,468
2018218812,562
2019156002,578
2020286102,618
20211811603,431
20222010313,945
20233110916,002
2024299006,047
20252110855,860
2026261221—

What is it indicated for?

FUJIFILM Video Laparoscope EL-R740S is intended to be used with a video processor, light source, monitor, hand instruments, electrosurgical unit and other ancillary equipment for minimally invasive observation, diagnosis and treatment in general abdominal, gynecologic and thoracic areas. The VP-7000 unit is used for endoscopic observation, diagnosis, treatment, and image recording. It is intended to process electronic signals transmitted from a video…

Read the full statement (225 words)

FUJIFILM Video Laparoscope EL-R740S is intended to be used with a video processor, light source, monitor, hand instruments, electrosurgical unit and other ancillary equipment for minimally invasive observation, diagnosis and treatment in general abdominal, gynecologic and thoracic areas.

The VP-7000 unit is used for endoscopic observation, diagnosis, treatment, and image recording. It is intended to process electronic signals transmitted from a video endoscope (a video camera in an endoscope). This product may be used on all patients requiring endoscopic examination and when using a Fujinon/FUJIFILM medical endoscope and light source together with monitor, recorder and various peripheral devices. BLI (Blue Light Imaging), LCI (Linked Color Imaging) and FICE (Flexible spectral-Imaging Color Enhancement) are adjunctive tools for gastrointestinal endoscopic examination which can be used to supplement Fujifilm white light endoscopy. BLI, LCI and FICE are not intended to replace histopathological sampling as a means of diagnosis.

The BL-7000 Light Source is used for endoscopic observation, diagnosis, treatment, and image recording. It is intended to provide illumination to an endoscope. The light source also functions as a pump to supply air through the endoscope while inside the body to assist in obtaining clear visualization to facilitate diagnostic examination. This product may be used on all patients requiring endoscopic examination and when using a Fujinon/FUJIFILM medical endoscope and video processor together with monitor, recorder and various peripheral devices.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192918: Video Laparoscope, Video Processor, Light Source.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192918

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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