(35 days)
No
The summary describes data acquisition, visualization, and analysis tools, but there is no mention of AI or ML being used for these functions. The "Mentions AI, DNN, or ML" field is explicitly marked as "Not Found".
No
The device is used for diagnostic and evaluation purposes by acquiring, visualizing, and analyzing pressure and impedance data within the gastrointestinal tract, not for therapy. It assists in the diagnosis of disorders.
Yes
The "Intended Use / Indications for Use" section explicitly states that the system's purpose includes "assisting in the diagnosis and evaluation of gastrointestinal and swallowing disorders," and the "Device Description" mentions "analytic diagnosis."
No
The device description explicitly states that the system includes a "catheter probe" with "pressure sensing element with Impedance sensor channels" and "interface electronics," indicating the presence of hardware components beyond just software.
Based on the provided information, the ManoScan Motility with Impedance Visualization System is not an In Vitro Diagnostic (IVD).
Here's why:
- IVDs analyze samples taken from the human body (e.g., blood, urine, tissue). The ManoScan system directly measures pressure and impedance within the gastrointestinal tract using a catheter inserted into the body.
- The device description and intended use clearly state it's used to acquire data in vivo (within the living body). It's a diagnostic tool that interacts directly with the patient's internal organs.
- The system provides visualization and analysis of in vivo measurements. While it assists in diagnosis, it does so by analyzing data collected directly from the patient's body, not from a sample processed outside the body.
Therefore, the ManoScan Motility with Impedance Visualization System falls under the category of a diagnostic medical device used for in vivo measurements, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The ManoScan Motility with Impedance Visualization System obtains a high resolution mapping of pressures and impedance levels within organs of the human gastrointestinal tract. These include the pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal organs. It is used in a medical clinical setting to acquire pressures, impedance levels and video and store the corresponding data. The system also provides visualization and analysis tools and information. The real time data as well as the analysis information can be viewed for diagnostic and analysis purposes with an intention of assisting in the diagnosis and evaluation of gastrointestinal and swallowing disorders.
Product codes (comma separated list FDA assigned to the subject device)
FFX
Device Description
The ManoScan Motility with Impedance Visualization System is used to acquire gastrointestinal tract data in order to present a high-resolution mapping of pressures with Impedance levels within tubular organs. It includes the ability to acquire, display and replay video data captured from within the gastrointestinal tract organs. The ManoScan Motility with Impedance Visualization can be used with either or both of the video with Impedance data capture features disabled.
The System is used in a medical clinical setting to sense pressure and Impedance levels, acquire and store the corresponding data and enable viewing or analyzing in real time or anytime after the data is acquired and stored. Accordingly, the System provides visualization and analysis tools that can be used for evaluation of the data and analytic diagnosis.
The system includes a catheter probe that can be configured with a variety of pressure sensing element with Impedance sensor channels. During the clinical procedure, the catheter is inserted transorally or via rectal intubation and pressure with Impedance levels from inside the gastrointestinal tract are monitored. Data collection can include acquisition of data from different segments of the GI tract, including the pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal area. Real-time data is sampled from each sensing channel via the interface electronics and made available to the software during each sample period. The software displays the data in real-time to support the clinical procedure.
The software also supports operational utility functions such as providing the user an interface for operating the pressure calibration pump. It obtains the cathere pressure sensor and calibration chamber data during the calibration process and determines the correction factors to be used in subsequent data collection.
The ManoScan Motility with Impedance Visualization system supports physician diagnosis and analysis by means of a playback / review function, which replays a stored session using previously recorded pressure, impedance and video data instead of real-time data. This analysis and diagnosis function is enabled through the presentation of pressure levels, gastrointestinal tract bolus presence, impedance levels and analysis, the impedance and video can be reviewed and analyzed in conjunction with pressure profiles and associated essimated parameters such as LES location, LES resting pressure, LES residual pressure, pressure inversion point (PIP) location, UES pressure, and esophageal motility such as amplitude duration and velocity.
The primary ManoScan Motility with Impedance Visualization functions are:
- Calibrate the pressure sensors .
- . Provide user interface displays, prompts, and controls
- Collect pressure, impedance and video data .
- Display, store and replay collected data .
- Provide analysis and diagnostic tools via software application .
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Video
Anatomical Site
pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal organs.
Indicated Patient Age Range
Not Found
Intended User / Care Setting
medical clinical setting, gastroenterologists, surgeons and medically trained personnel.
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Bench-top Verification Tests have been performed to verify product performance meets or exceeds performance of the predicate devices. This has included pressure with Impedance accuracy, noise and repeatability measurement tests performed as part of the Design Verification and Validation process.
No formal clinical testing has been performed, nor is any believed to be necessary.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 876.1725 Gastrointestinal motility monitoring system.
(a)
Identification. A gastrointestinal motility monitoring system is a device used to measure peristalic activity or pressure in the stomach or esophagus by means of a probe with transducers that is introduced through the mouth into the gastrointestinal tract. The device may include signal conditioning, amplifying, and recording equipment. This generic type of device includes the esophageal motility monitor and tube, the gastrointestinal motility (electrical) system, and certain accessories, such as a pressure transducer, amplifier, and external recorder.(b)
Classification. Class II (performance standards).
0
K091070
PAGE 1 OF 5
SIERRA SCIENTIFIC
INSTRUMENTS
510(k) Summary
| Identification: | |
|---|---|
| Date: | April 3rd, 2009 |
| MAY 19 2009 | |
| Applicant's/Owner's Name: | Sierra Scientific Instruments, Inc. |
| Phone number: | 310.641.8492 |
| Fax number: | 310.872.5558 |
| Submission Contact person: | Eric S. Finkelman |
| Phone number: | 310.641.8492 |
| Fax number: | 310.872.5558 |
| Manufacturing site address: | Sierra Scientific Instruments, Inc. |
| 5757 West Century Boulevard | |
| Suite 660 | |
| Los Angeles, CA 90045 | |
| Device Trade Name: | Gastrointestinal Motility System (Electrical) |
| Proprietary Name: | ManoScan Motility with Impedance Visualization System |
| Device classification: | Class II |
| Panel / Regulation Number: | 876.1725 |
| Product Code | FFX |
| Establishment registration number: | 3005344223 |
Substantial equivalence claimed to:
- K031169 Sierra Scientific Instruments, Inc. Motility Visualization System; ManoScan 1.
- K984444 / K012232 Sandhill Scientific Instruments, Inc InSight Motility Visualization System 2.
- K052338 Medical Measurement Systems B.V .- Solar GI High Resolution Manometry with Impedance 3. System
Description:
The ManoScan Motility with Impedance Visualization System is used to acquire gastrointestinal tract data in order to present a high-resolution mapping of pressures with Impedance levels within tubular organs. It includes the ability to acquire, display and replay video data captured from within the gastrointestinal tract organs. The ManoScan Motility with Impedance Visualization can be used with either or both of the video with Impedance data capture features disabled.
The System is used in a medical clinical setting to sense pressure and Impedance levels, acquire and store the corresponding data and enable viewing or analyzing in real time or anytime after the data is acquired and stored. Accordingly, the System provides visualization and analysis tools that can be used for evaluation of the data and analytic diagnosis.
The system includes a catheter probe that can be configured with a variety of pressure sensing element with Impedance sensor channels. During the clinical procedure, the catheter is inserted transorally or via rectal intubation and pressure with Impedance levels from inside the gastrointestinal tract are monitored. Data collection can include acquisition of data from different segments of the GI tract, including the pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal area. Real-time data is sampled from each sensing channel via the interface electronics and made available to the software during each sample period. The software displays the data in real-time to support the clinical procedure.
1
K091070
PAGE 2 OF 5
Sierra Scientific
INSTRUMENTS
in davinstic rachaalown
Image /page/1/Figure/2 description: This image shows a diagram of a system with several components. The components include a computer, impedance acquisition electronics, pressure acquisition electronics, a pump, a manometric and impedance catheter, and a calibration pressure chamber. The diagram also includes two boxes labeled A200 and A100, which appear to be connected to the other components.
ManoScan Motility with Impedance Visualization System Typical System Overview
The software also supports operational utility functions such as providing the user an interface for operating the pressure calibration pump. It obtains the cathere pressure sensor and calibration chamber data during the calibration process and determines the correction factors to be used in subsequent data collection.
The ManoScan Motility with Impedance Visualization system supports physician diagnosis and analysis by means of a playback / review function, which replays a stored session using previously recorded pressure, impedance and video data instead of real-time data. This analysis and diagnosis function is enabled through the presentation of pressure levels, gastrointestinal tract bolus presence, impedance levels and analysis, the impedance and video can be reviewed and analyzed in conjunction with pressure profiles and associated essimated parameters such as LES location, LES resting pressure, LES residual pressure, pressure inversion point (PIP) location, UES pressure, and esophageal motility such as amplitude duration and velocity.
Product Functions
The primary ManoScan Motility with Impedance Visualization functions are:
- Calibrate the pressure sensors .
- . Provide user interface displays, prompts, and controls
- Collect pressure, impedance and video data .
- Display, store and replay collected data .
- Provide analysis and diagnostic tools via software application .
Intended use:
The ManoScan Motility with Impedance Visualization obtains a high resolution mapping of pressures with Impedance levels within organs of the human gastrointestinal tract. These include the pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal organs. It is used in a medical clinical setting to acquire pressures, impedance levels and video, to aid in documenting and diagnosing motility, digestive tract and swallowing disorders. The system also provides visualization and analysis tools and reports that can be viewed for diagnostic purposes by appropriately trained medical personnel.
The system includes a catheter probe that can be configured with a variety of pressure sensing elements with Impedance sensor channels. During the clinical procedure, the catheter is inserted transnasally, transorally or via rectal intubation and pressure with Impedance levels from inside the gastrointestinal tract are monitored
SIERRA SCIENTIFIC INSTRUMENTS, INC. • 5757 CENTURY BOULEVARD, SUITE 660 • LOS ANGELES, CA 90045
WWW.SIERRAINST.COM
Fax: 310.872.5558
PHONE: 310 641.8492
2
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Summary of Technological Characteristics:
The ManoScan Motility with Impedance Visualization System catheter represents a modification to the predicate Sierra Scientific Instruments, Inc. Motility Visualization System; ManoScan pressure sensing catheter. The primary difference is the addition of cylindrical gold conductive rings that create impedance measurement electrodes, when impedance is enabled. Configurations of the subject device will also vary the number of pressure sensors (typically 8 - 36 for the predicate device). The ManoScan Motility with Impedance Visualization System uses a multiplexing scheme to minimize the number of electrical conductors.
The ManoScan Motility with Impedance Visualization System includes separate modules for acquisition of the impedance and pressure data. Both acquisition modules communicate with the data acquisition software via a standard computer platform. Video is captured via standard video capture devices and synchronized within the software application.
The user interface is via touch screen display, keyboard and the use of a hard drive that allows recording and play back of the data. By providing more data, the system gives a more complete pressure, impedance and video data set of the segment of the gastrointestinal tract being investigated. The system can also be used if there are inactive sensors or channels and can be configured with different combinations of the pressure, impedance and video capabilities.
Substantial Equivalence - Summary of Technical Similarities / Differences with Predicate Devices:
As mentioned above, the ManoScan Motility with Impedance Visualization System hardware architecture is identical to the predicate Motility Visualization System; ManoScan device with the only system difference being that the ManoScan Motility with Impedance Visualization System device includes for auxiliary data like impedance and video. This modules are designed to communicate directly with the software, along with the pressure data acquisition module. As with the predicate devices, the ManoScan Motility with Impedance Visualization System includes a communication link between the data acquisition modules and a computer which hosts the acquisition and analysis software.
The MaroScan Motility with Impedance Visualization System catheter uses the same proprietary capacitive tactile pressure sensor technology utilized in the predication System; ManoScan device to provide circumferential pressure sensing along the active length of the catheter. Pressure sensors are presented in an array similar to the predicate Motility Visualization System; ManoScan device, with certain configurations of the ManoScan Motility with Impedance Visualization System device providing higher density pressure arrays to provide greater measurement resolution.
Additionally, the ManoScan Motility with Impedance Visualization System catheter includes impedance electrodes which are not present in the predication System; ManoScan device but have the same technological characteristics as the predicate catheters provided with the InSight and Solar GI devices referenced. More specifically, the ManoScan Motility with Impedance Visualization System catheter includes impedance electrodes which are integrated into the catheter via a core catheter construction that is identical to the predicate Motility with Impedance Visualization System; ManoScan device and are presented as conductive rings. Each pair of rings creates an impedance channel. This is identical in technology approach as the predicate Insight and Solar GI devices. Aside from the core catheter construction and the pressure sensing technology utilized in the applicant ManoScan, which is identical to the predicate Motility Visualization System; ManoScan device, the primary technology differences with the predicate Insight and Solar GI impedance devices is the impedance electrode material, the number of impedance electrodes and channels as well as the relative location of the impedance electrodes. As compared to these predicate devices, the ManoScan Motility with Impedance Visualization System device uses an impedance electrode ring design which provides equivalent or better impedance measurement effectiveness and enables catheter configurations and data acquisition modules that support a higher number of pressure with Impedance sensors to improve pressure with Impedance signal measurement coverage and resolution.
The ManoScan Motility with Impedance Visualization System device supports video data capture and analysis with similar technological characteristics as the predicate Solar GI device.
3
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Finally, the ManoScan Motility with Impedance Visualization System is designed and certified to be in accordance with the same applicable standards and non-clinical tests as the predicate Motility Visualization System; ManoScan pressure measurement device, and the Insight and Solar GI pressure with Impedance devices. Additionally, the ManoScan Motility with Impedance Visualization System is designed with a target customer base similar to the predicate ManoScan, Insight and Solar GI devices.
Summary of Hardware / Software Components
Acquisition Hardware – This subsystem, manufactured by Sierra Scientific Instruments, Inc., includes data acquisition modules that are used for power control, calibration control and processing the electrical, video, pressure with Impedance and auxiliary data signals while providing the necessary electrical isolation for safety.
Catheter Assembly including Sensors and Electrodes – the sensors and electrodes included in the catheter assembly are used for generating data signals in response to physiological events to which they are exposed. They are manufactured by Sierra Scientific Instruments, Inc. The catheter, sensors and electrodes are assembled and tested in such a manner as to meet or exceed the necessary patient safety requirements and meet or exceed the performance characteristics of the predicate devices.
Acquisition and Analysis Software - the software controls the calibration procedure, clinical procedure protocol, and provides analysis tools while providing visualization tools that can be used during the procedure, analysis or in generating reports. The software includes warnings and visual indicators that alert users if product performance or operating conditions are not meeting performance requirements. The software is developed by Sierra Scientific Instruments, Inc. and is verified and validated to ensure the product meets or exceeds the performance characteristics of the predicate devices.
Applicable Standards and Non-Clinical Testing
In accordance with Sierra Scientifics Instruments' Product Realization procedures, the ManoScan Motility with Impedance Visualization System has been designed and verified to meet the appropriate elements of the following standards:
IEC 60601-1:1988 + A1:1991 + A2:1995 EN 60601-1-2 AND IEC 60601-1-2 ISO 10993
Certification to the above standards is achieved through a combination of internal design documentation and external lab testing against approved protocols. Specifically, the above confirm adherence to the appropriate levels of product safety, emissions, voltage immunization and biocompatibility.
Bench-top Verification Tests have been performed to verify product performance meets or exceeds performance of the predicate devices. This has included pressure with Impedance accuracy, noise and repeatability measurement tests performed as part of the Design Verification and Validation process.
No formal clinical testing has been performed, nor is any believed to be necessary.
Safety and Potential Adverse Health Effects
The ManoScan Motility with Impedance Visualization System has been designed to completely eliminate or mitigate all known health hazards associated with use of the device. Health hazard risk reduction has been achieved through application of a rigorous risk management program that is included as part of the Sierra Scientific Instruments, Inc. design process and documents as part of the device Safety Risk Analysis. One or more of the following was used to mitigate the health hazards identified by the risk management program:
- Design Verification and Validation Testing and Certification to Applicable Standards 1.
- Material / Product Conformance Inspection and Acceptance Testing Criteria 2.
4
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Innovadons in diugnostic technology."
- Detection of hazardous or non-conforming conditions via software and alerting the user through alarms and visual indicators.
- Identification of health hazard conditions and related cautions in the instruction manual and other device 4. labeling
- Training of qualified personnel to perform procedures and interpret results. న్.
Sierra Scientific Instruments, Inc believes that the ManoScan Motility with Impedance Visualization System is a safe and effective device and has been proven to meet or exceed the performance and safety levels of the legally marketed Motility Visualization System; ManoScan, Insight and Solar GI predicate devices.
5
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/5/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal features a stylized eagle with three tail feathers, representing the department's commitment to health, human services, and well-being. The eagle is encircled by the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement.
Public Health Service
MAY. 19 2009
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Sierra Scientific Instruments, Inc. c/o Mr. Jeffrey D. Rongero Senior Project Engineer UL Health Sciences Underwriters Laboratories, Inc. 12 Laboratory Drive RESEARCH TRIANGLE PARK NC 27709
Re: K091070
Trade/Device Name: ManoScan Motility with Impedance Visualization System Regulation Number: 21 CFR §876.1725 Regulation Name: Gastrointestinal motility monitoring system Regulatory Class: II Product Code: FFX Dated: May 1, 2009 Received: May 4, 2009
Dear Mr. Rongero:
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 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. 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.
6
Page 2
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Center for Devices and Radiological Health's (CDRH's) Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter.
| 21 CFR 876.xxx | (Gastroenterology/Renal/Urology) | (240) 276-0115 |
|---|---|---|
| 21 CFR 884.xxx | (Obstetrics/Gynecology) | (240) 276-0115 |
| 21 CFR 892.xxx | (Radiology) | (240) 276-0120 |
| Other | (240) 276-0100 |
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please contact the CDRH/Office of Surveillance and Biometrics/Division of Postmarket Surveillance at 240-276-3464. For more information regarding the reporting of adverse events, please go to http://www.fda.gov/cdrh/mdr/.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
[signature]
Janine M. Morris Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
7
Indications for Use
510(k) Number (if known):
Device Name: ManoScan Motility with Impedance Visualization System
Indications For Use:
The ManoScan Motility with Impedance Visualization System obtains a high resolution mapping of pressures and impedance levels within organs of the human gastrointestinal tract. These include the pharynx, upper esophageal sphincter (UES), esophagus, lower esophageal sphincter (LES), stomach, sphincter of oddi, small bowel, colon, duodenum and anorectal organs. It is used in a medical clinical setting to acquire pressures, impedance levels and video and store the corresponding data. The system also provides visualization and analysis tools and information. The real time data as well as the analysis information can be viewed for diagnostic and analysis purposes with an intention of assisting in the diagnosis and evaluation of gastrointestinal and swallowing disorders. The device is intended for use by gastroenterologists, surgeons and medically trained personnel.
| Prescription Use | X |
|---|---|
| (Part 21 CFR 801 Subpart.D) |
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) ..
Concurrence of CDRH, Office of Device Evaluation (ODE
Ami M. Whitney
(Division Sign-Off)
lon of Reproductive, Abdominal and Radiological Devices 510(k) Number
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