Processor VP-7000, Light Source BL-7000

K163675 · Fujifilm Medical System U.S.A., Inc. · FET · Apr 25, 2017 · Gastroenterology, Urology

Device Facts

Record IDK163675
Device NameProcessor VP-7000, Light Source BL-7000
ApplicantFujifilm Medical System U.S.A., Inc.
Product CodeFET · Gastroenterology, Urology
Decision DateApr 25, 2017
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 876.1500
Device ClassClass 2

Intended Use

Processor VP-7000 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. Light Source BL-7000 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.

Device Story

System comprises VP-7000 Video Processor and BL-7000 Light Source; used with Fujinon/FUJIFILM endoscopes. Processor receives electronic signals from endoscope camera; performs image processing including white light, FICE, BLI, BLI-bright, and LCI; outputs video to monitor/recorder. Light source provides LED illumination and air pump function for body cavity visualization. Used in clinical settings by medical practitioners. BLI/LCI/FICE serve as adjunctive tools for gastrointestinal examination to supplement white light imaging; intended to enhance visualization of micro-vessels and mucous color. Output aids clinicians in diagnostic examination; does not replace histopathological sampling. System supports bi-directional communication with EMR systems.

Clinical Evidence

Prospective clinical reader study; sample size not specified. Compared BLI and BLI-bright presets against FICE (K140149) using 4-point Likert scale for image quality across various GI anatomic locations. Results established substantial equivalence of diagnostic visualization to predicate.

Technological Characteristics

Steel-polycarbonate housing; 4 LED lamp light source (79.2W); AC powered (100-240V). Connectivity: HD-SDI, DVI, Ethernet, bi-directional EMR communication. Image processing: FICE, BLI, BLI-bright, LCI. Software: Proprietary spectral/structural enhancement algorithms. Electrical safety per IEC 60601; software validation per IEC 62304.

Indications for Use

Indicated for all patients requiring endoscopic examination for observation, diagnosis, treatment, and image recording using Fujinon/FUJIFILM endoscopes. No specific age or gender contraindications stated.

Regulatory Classification

Identification

An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

Special Controls

*Classification* —(1)*Class II (special controls).* The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is an abstract symbol that resembles an eagle or a stylized human figure. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 April, 25, 2017 FUJIFILM Medical System U.S.A., Inc. Shraddha S More Specialist. Regulatory Affairs and Quality Assurance 10 High Point Drive Wayne, NJ 07470 Re: K163675 Trade/Device Name: FUJIFILM Processor VP-7000 and Light source BL-7000 Regulation Number: 21 CFR§ 876.1500 Regulation Name: Endoscope and Accessories Regulatory Class: II Product Codes: FET, NTN, NWB, PEA Dated: March 21, 2017 Received: March 21, 2017 Dear Shraddha S More: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. {1}------------------------------------------------ You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely, # Benjamin R. Fisher -S Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K163675 Device Name FUJIFILM Processor VP-7000 and Light source BL-7000 Indications for Use (Describe) Processor VP-7000 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. Light Source BL-7000 The BL-7000 Light Source is used for endoscopic observation, diagnosis, treatment, and image recording, If 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 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. | Type of Use (Select one or both, as applicable) | | |------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | <div> <span> <svg height="12" width="12"> <rect fill="none" height="12" stroke="black" stroke-width="1" width="12" x="0" y="0"></rect> <line stroke="black" stroke-width="1" x1="0" x2="12" y1="0" y2="12"></line> <line stroke="black" stroke-width="1" x1="0" x2="12" y1="12" y2="0"></line> </svg> </span> Prescription Use (Part 21 CFR 801 Subpart D) </div> | <div> <span> <svg height="12" width="12"> <rect fill="none" height="12" stroke="black" stroke-width="1" width="12" x="0" y="0"></rect> </svg> </span> Over-The-Counter Use (21 CFR 801 Subpart C) </div> | CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. ## *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ ## 510(k) SUMMARY ## FUJIFILM Processor VP-7000 and Light Source BL-7000 ## Date: March 21, 2017 ## Submitter's Information FUJIFILM Medical Systems U.S.A., Inc., Endoscopy Division 10 High Point Drive Wayne, NJ 07470 USA FDA Establishment Registration Number: 2431293 ## Contact Person: Shraddha More Specialist, Regulatory Affairs and Quality Assurance Telephone: (973) 686-2627 Facsimile: (973) 633-8818 E-Mail: smore@fujifilm.com ## Identification of the Proposed Device: Proprietary/Trade Name: Common Name: Device Class: Review Panel: FUJIFILM Processor VP-7000 and Light Source BL-7000 Endoscopic Video Imaging System/Component Class II Gastroenterology and Urology Classification Information: | Classification Name | CFR Section | Product Codes | |-------------------------------------------------------------------------|-----------------|---------------| | Endoscopic Video Imaging System/Component,<br>Gastroenterology- Urology | 21 CFR 876.1500 | FET | | Led Light source, Endoscope and accessories | 21 CFR 876.1500 | NTN | | Endoscope and accessories, Narrow Band<br>Spectrum | 21 CFR 876.1500 | NWB | | Endoscope, Accessories, Image Post-Processing<br>For Color Enhancement | 21 CFR 876.1500 | PEA | ## Predicate Device - Primary: Fujifilm EPX-4440HD Digital Video Processor with FICE and Light Source ● (K140149) - Secondary: Olympus Video System Center CV-170 (K122831) ● {4}------------------------------------------------ ## Device Description VP-7000 and BL-7000 are intended to be used in conjunction with Fujinon/FUJIFILM endoscopes for endoscopic observation, diagnosis, treatment, and image recording. The description for each of the components of the subject device is below: ## The VP-7000 Video Processor: The Processor relays the image from the endoscope to a video monitor. Projection can be either analog or digital at the user's preference. The Processor incorporates internal digital storage capacity. The Processor also controls the light projected to the body cavity. The Processor provides for optional structural enhancement through user modes FICE. BLI. BLI-bright and LCI. Spectral and structural enhancements are achieved through proprietary software. The device is AC operated at a power setting of 100-240V/50-60Hz/0.8-0.5A. The Processor is housed in a steelpolycarbonate case measuring 390x110x485mm. The DK-7000E Keyboard is a standard accessory of VP-7000. It is used to enter pertinent procedural information (patient, physician, date, etc.) for display on the video monitor and digital/analog storage systems. The Keyboard is also used to control operational features of the VP-7000 Processor. The Keyboard resembles a standard computer keyboard, and is provided with an instruction label attached to it. ## The BL-7000 Light Source: The Fujinon/FUJIFILM endoscope employs fiber bundles to transmit light from the light source and subsequently to the body cavity. The Light Source employs 79.2W 4 LED lamps. Brightness control is performed by the user. The device is AC operated at a power setting of 100-240V/50-60Hz/1.2-0.7A. The Light Source is housed in a steel-polycarbonate case measuring 390x155x485mm. ## Intended Use / Indications for Use ## Processor VP-7000 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 qastrointestinal 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. ## Light Source BL-7000 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. {5}------------------------------------------------ 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. ## Summary of Technological Characteristics The differences between the technological characteristics of the subject device and predicate devices are provided in the table below. VP-7000 and BL-7000 are the same as the cleared EPX-4440HD Digital Video Processor with FICE and Light source (K140149) device, with the exception of additional image processing options termed as "BLI" (Blue Light Imaging) and LCI (Linked Color Imaging) for providing image enhanced endoscopy adjunct to white light imaging (WLI). As with the EPX-440HD predicate device, the subject processor receives an image from the endoscope via a connector cable. The subject processor is capable of bi-directional communication that allows importation of various patient and procedural data between EMR (Electronic Medical Record) systems. BLI and LCI are image processing features that a licensed medical practitioner (user) can utilize, as adjunctive tools, to supplement the white light endoscopic examination. The BLI and LCI features of VP-7000 and BL-7000 use narrow band short wavelength LED lights for outputting the spectrum image. BLI mode produces higher-contrast images of micro vessels by increasing the intensity ratio of the Violet LED light relatively as compared with WLI mode. BLI-bright mode can create brighter images than BLI, by slightly decreasing the intensity ratio of the Violet LED light relatively as compared with WLI mode. LCI mode produces enhanced mucous color by signal processing and increases the ratio of the Violet LED light relatively as compared with WLI mode. The technological characteristics of BL-7000 are substantially equivalent to the predicate EPX-4440HD light source, except that it uses LED lights (like the CV-170) rather than Xenon lights. ## Performance Data ## Non-clinical testing: VP-7000 and BL-7000 have no potential for patient contact. Therefore, biocompatibility testing for the subject device is not applicable. Testing of the VP-7000 consisted of software validation in accordance with IEC 62304 and electrical safety in accordance with IEC 60601 requirements. Functional testing of the FICE, BLI-bright and LCI image processing features included Contrast Enhancement (or Color and Contrast Enhancement), Resolving Power, Noise, Artifact Creation, and Color Reproduction. All testing criteria were met, and in all instances the device functioned as intended. ## Clinical testing: The BLI and BLI-bright features were evaluated in a prospective clinical trial to objectively assess the overall image quality of each of the BLI and BLI-bright presets in comparison to the FICE presets (K140149). The study design was a reader concurrence study designed in accordance with the FDA document "Guidance on Solid State X-ray Imaging Devices" and consisted of two parts: (1) acquisition of images; and (2) reader study. Each subject (patient) underwent an endoscopic examination using VP-7000 Video Processor. BL-7000 Light Source and FUJIFILM's video endoscopes during a single clinical procedure, first with white light imaging (WLI), followed by an {6}------------------------------------------------ examination with FICE, BLI and BLI-bright imaging. The images were taken from different anatomic locations within the gastrointestinal tract (i.e., colon, duodenum, esophagus, or gastric region), and analyzed independently by multiple blinded investigators using a 4-point Likert scale. The clinical study established that BLI and BLI-bright demonstrated substantial equivalence of diagnostic visualization (e.g. image quality) to the predicate FICE. ## Conclusions FUJIFILM Processor VP-7000 and Light Source BL-7000 are substantially equivalent to their predicate devices, the EXP-4440HD Digital Video Processor with FICE and Light Source system (K140149) and the Olympus Video System Center CV-170 (K122831). VP-7000 and BL-7000 have the same intended use and similar indications, technological characteristics, and principles of operation as their predicate devices. The minor technological differences between VP-7000 and BL-7000 and their predicate devices raise no new issues of safety or effectiveness. Performance data demonstrate that Processor VP-7000 and Light Source BL-7000 are as safe and effective as the EXP-4440HD Digital Video Processor with FICE and Light source. Thus, VP-7000 and BL-7000 are substantially equivalent to their predicate devices. | Device | Parameters | Primary<br>Predicate:<br>Fujifilm EPX-<br>4440HD Digital<br>Video Processor<br>with FICE and<br>Light Source | Secondary Predicate:<br>OLYMPUS CV-170<br>VIDEO CENTER | Subject Device:<br>FUJIFILM processor<br>VP-7000 and Light<br>source BL-7000 | |---------------------|------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 510(k) number | | K140149 | K122831 | K163675 | | Indications for Use | | The VP-4440 HD<br>unit is used for<br>endoscopic<br>observation,<br>diagnosis,<br>treatment, and<br>image recording. It<br>is intended to<br>process electronic<br>signals transmitted<br>from a video<br>endoscope (a<br>video camera in an<br>endoscope). This<br>product may be<br>used on all patients<br>requiring<br>endoscopic<br>examination and<br>when using a<br>Fujinon/Fujifilm<br>medical | This video system center<br>is intended to be used<br>with OLYMPUS video<br>converter, camera heads,<br>endoscopes, monitors,<br>EndoTherapy<br>accessories, and other<br>ancillary equipment for<br>endoscopic diagnosis,<br>treatment, and video<br>observation. | Processor VP-7000<br>The VP-7000 unit is<br>used for endoscopic<br>observation, diagnosis,<br>treatment, and image<br>recording.<br>It is intended to process<br>electronic signals<br>transmitted from a video<br>endoscope (a video<br>camera in an<br>endoscope).<br>This product may be<br>used on all patients<br>requiring endoscopic<br>examination and when<br>using a<br>Fujinon/FUJIFILM | | Device | Parameters | Primary<br>Predicate:<br>Fujifilm EPX-<br>4440HD Digital<br>Video Processor<br>with FICE and<br>Light Source | Secondary Predicate:<br>OLYMPUS CV-170<br>VIDEO CENTER | Subject Device:<br>FUJIFILM processor<br>VP-7000 and Light<br>source BL-7000 | | | | endoscope, light<br>source, monitor,<br>recorder and<br>various peripheral<br>devices. FICE is an<br>adjunctive tool<br>which can be used<br>to supplement<br>FUJIFILM white<br>light endoscopy.<br>FICE is not<br>intended to replace<br>histopathological<br>sampling as a<br>means of<br>diagnosis. | | medical endoscope and<br>light source together<br>with monitor, recorder<br>and various peripheral<br>devices.<br><br>BLI (Blue Light<br>Imaging), LCI (Linked<br>Color Imaging) and<br>FICE (Flexible spectral-<br>Imaging Color<br>Enhancement) are<br>adjunctive tools for<br>gastrointestinal<br>endoscopic examination<br>which can be used to<br>supplement Fujifilm<br>white light endoscopy.<br><br>BLI, LCI and FICE are<br>not intended to replace<br>histopathological<br>sampling as a means of<br>diagnosis.<br><br><b>Light Source BL-7000</b><br>The BL-7000 Light<br>Source is used for<br>endoscopic observation,<br>diagnosis, treatment,<br>and image recording. It<br>is intended to provide<br>illumination to an<br>endoscope.<br><br>The light source also<br>functions as a pump to<br>supply air through the<br>endoscope while inside<br>the body to assist in<br>obtaining clear<br>visualization to facilitate<br>diagnostic examination.<br>This product may be | | Device | Parameters | Primary<br>Predicate:<br>Fujifilm EPX-<br>4440HD Digital<br>Video Processor<br>with FICE and<br>Light Source | Secondary Predicate:<br>OLYMPUS CV-170<br>VIDEO CENTER | Subject Device:<br>FUJIFILM processor<br>VP-7000 and Light<br>source BL-7000 | | | | | | used on all patients<br>requiring endoscopic<br>examination and when<br>using a<br>Fujinon/FUJIFILM<br>medical endoscope and<br>video processor<br>together with monitor,<br>recorder and various<br>peripheral devices. | | Processor | | VP-4440HD | CV-170 | VP-7000 | | | Power Rating | 120V AC<br>60Hz<br>0.8A | 100-240V AC<br>50/60Hz<br>200VA | 100-240V AC<br>50/60Hz<br>0.8-0.5A | | | Compatible<br>Endoscope | 400 System Scope<br>500 System Scope<br>600 System Scope | 100/130/140/150/160/180<br>Series and GI/BF/VISER<br>A Series scope | 500 System Scope<br>600 System Scope<br>700* System Scope (not<br>available in USA) | | | Keyboard | DK-4440E | MAJ-1981 | DK-7000E | | | Bi-Direction<br>communication | Available | Unknown | Available | | | Peripheral | Printer | Printer | Printer | | | Digital Output | HD-SDI:HDTV<br>1080i<br>DVI(Digital Visual<br>Interface)<br>Ethernet | HD-SDI<br>SD-SDI<br>DVI(Digital Visual<br>Interface) | HD-SDI:HDTV 1080i<br>DVI(Digital Visual<br>Interface)<br>Ethernet | | | Analog Output | RGB, Y/C,<br>Composite | RGB, Y/C, Composite,<br>Y/PbPr, VBS | RGB, Y/C, Composite | | | Analog Input | Not available | Not available | Composite | | | Color<br>Adjustment | Black, Red, Green,<br>Blue, R-Hue,<br>Chroma; 9steps | Red, Blue, Chroma;<br>±8steps | Black, Red, Green,<br>Blue, R-Hue, Chroma;<br>9steps | | | Enhancement | Hyper-Sharpness<br>(Structure<br>enhance)<br>Color Enhance | | Hyper-Sharpness<br>(Structure enhance)<br>Color Enhance | | | FICE | Available | Not available | Available | | | BLI | Not available | Not available | Available with E-600HL,<br>EC-600LS, EG-600WR | | Device | Parameters | Primary<br>Predicate:<br>Fujifilm EPX-<br>4440HD Digital<br>Video Processor<br>with FICE and<br>Light Source | Secondary Predicate:<br>OLYMPUS CV-170<br>VIDEO CENTER | Subject Device:<br>FUJIFILM processor<br>VP-7000 and Light<br>source BL-7000 | | | BLI-bright | Not available | Not available | Available with E-600HL,<br>EC-600LS, EG-600WR<br>v2, and EC-600WL v2<br>and 700* series<br>endoscopes | | | LCI | Not available | Not available | Available with E-600HL,<br>EC-600LS, EG-600WR<br>v2, and EC-600WL v2<br>and 700* series<br>endoscopes | | | Iris | Average/Peak/Auto | Average/Peak/Auto | Average/Peak/Auto | | | Peak<br>Detection level | Available | Unknown | Available | | | Shutter Speed | 1/800 Max | Unknown | 1/800 Max | | | Shutter Speed<br>Priority Mode | Available | Unknown | Available | | | Default Pump<br>Level<br>Selection | Off/L/M/H | High, Low, Off | Off/L/M/H | | | Mask Type | Type1/Type2 | Unknown | Type1/Type2 | | | Image Storage | External Device<br>and CF Card<br>(Max16GB) | MAJ-1925 Olympus 2GB<br>USB Portable Memory | External USB Memory<br>(Max 2GB) and Internal<br>Storage Memory | | | Dimensions<br>WxHxD mm | 390x105x460 mm | 295x145x425 mm | 390x110x485 mm | | | Weight | 9.5kg | 11kg | 9kg | | Light<br>Source | | XL-4450 | CV-170 | BL-7000 | | | Power Rating | 120V AC | 100-240V AC | 100-240V AC | | | | 60Hz | 50/60Hz | 50/60Hz | | | | 3.3A | 200VA | 1.2-0.7A | | | Lamp (power<br>consumption) | Main Lamp: Xenon<br>lamp (300W)…
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