ICS Dizcovery is used in the assessment of the vestibular-ocularreflex (VOR) and nystagmus by measuring, recording, displaying, and analyzing eye and head movements.

The 1091 ICS Dizcovery is used in the assessment of patients with complaints of a vestibular nature such as dizziness, disequilibrium, and vertigo. The ICS Dizcovery type 1091 does not treat or diagnose the patient; the diagnosis is determined by the credentialed physician.

ICS Dizcovery system is intended to be used by qualified medical personnel. Typical device users are Neurologists, Ears, Nose, and Throat specialists (ENTs), Audiologists, Physical Therapists, and Technicians supervised by one of the four mentioned typical users. Professionals with knowledge of diagnosing balance disorders. Users are assumed to have prior knowledge of the medical and scientific facts underlying the procedures offered by the ICS Dizcovery system.

The intended patient population are children in the age of 10 to 18 and adults in age range from 18 to 99 years with a complaint of dizziness, balance disorder, or vestibular disease.

Device Description

The ICS Dizcovery device is a portable video-oculography (VOG) device. The device shall be indicated for videonystagmography for the assessment of patients with complaints of dizziness, disequilibrium, and vertigo. It provides an assessment of the vestibular-ocular reflex (VOR) and nystagmus by measuring, recording, displaying, and analyzing eye and head movements.

The ICS Dizcovery is a wearable measurement system in the form of goggles, with built-in cameras and a motion sensor that simultaneously track eye- and head-movement, respectively. The goggles have two cameras that collect the eye movement video. The goggle device is connected to a PC with Otosuite Vestibular PC software (through a USB cable). The Otosuite Vestibular software functions by processing the binocular camera data collection. The collection of eye movement data is analysed to eye movement in respect to various stimuli throughout testing.

The ICS Dizcovery system is made up of the following components:

A pair of binocular video goggles for testing, controlled through the Otosuite Vestibular PC software
Otosuite Vestibular PC software for controlling tests, displaying test data for the various ● tests, reviewing, and printing test results, as well as and managing patients and patient data, users, and test devices.
A set of Shadeshift® Vision Denied panels; these panels deny the patients vision throughout ● testing whilst allowing the clinician to continue tracking the eyes in darkness. Vision denied testing is needed throughout the test workflow.
. A set of LCD panels; these automatically shift between dark states to facilitate a userfriendly approach to Skew Deviation testing. This removes the need for manually denying vision of each eye separately with the use of a hand or a paddle.
A face cushion which inserts into the goggle frame to promote comfort whilst wearing and allow a better fit to face.

AI/ML Overview

Here's a breakdown of the acceptance criteria and study information for the ICS Dizcovery device, based on the provided text:

1. Table of Acceptance Criteria and Reported Device Performance

Feature/Test	Acceptance Criteria	Reported Device Performance
Test Methods
Biocompatibility (Cytotoxicity, Sensitization, Irritation)	No issues found upon testing	No issues were found during biocompatibility testing.
Electrical Safety (IEC 60601-1:2005+AMD1:2012+AMD2:2020)	Compliance with standard	The ICS Dizcovery system was tested to and complies with this standard.
EMC (IEC 60601-1-2:2014+AMD1:2020, IEC 60601-4-2 Ed. 1.0 (2016))	Compliance with standards	The ICS Dizcovery system was tested to and complies with these standards.
Usability (IEC 60601-1-6:2010+A1:2013+A2:2020, IEC 62366-1:2015+AMD1:2020)	Compliance with standards	The ICS Dizcovery system was tested to and complies with these standards.
Software Lifecycle (IEC 62304:2006 + A1:2015)	Compliance with standard and FDA guidance	Software Verification and Validation testing were conducted, and Basic Documentation Level was provided as recommended by FDA's Guidance.
Laser Safety (IEC 60825-1:2014+ISH1:2017+ISH2:2017)	Compliance with standard	The ICS Dizcovery system was tested to and complies with this standard.
Photobiological Safety (IEC 62471:2006)	Compliance with standard	The ICS Dizcovery system was tested to and complies with this standard.
Basic Vestibular Function Testing (ANSI S3.45-2009 (Reaffirmed 2019))	Compliance with standard	The ICS Dizcovery system was tested to and complies with this standard.
Mechanical Testing (Goggle stimuli projection system, Scratch resistance of mirror, Head strap pull cycle, USB cable bend and pull cycle)	Performance not degraded over useful lifetime	The ICS Dizcovery successfully underwent mechanical testing to ensure that the performance of the device is not degraded by wear and tear over its useful lifetime.
Design Verification & Validation	All tests meet required acceptance criteria	All tests were verified to meet the required acceptance criteria. The performance testing demonstrated that the differences in the design and performance do not affect intended use or raise new questions on safety and effectiveness.

2. Sample Size Used for the Test Set and Data Provenance

The document does not explicitly state the sample size for any specific test sets. However, it does refer to "Design Verification & Validation activities" and "Reliability testing... conducted... by a third party." It does not provide information about the country of origin of the data or whether it was retrospective or prospective.

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts

This information is not provided in the document. The document mentions that a "credentialled physician will use this data to make a diagnosis," but this refers to the intended use of the device, not the establishment of ground truth for testing.

4. Adjudication Method for the Test Set

This information is not provided in the document.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done, and the Effect Size

No MRMC comparative effectiveness study is mentioned in the provided text. The document focuses on demonstrating substantial equivalence to a predicate device through non-clinical performance data and technical comparisons.

6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) Was Done

The document implies standalone performance testing as part of the "Software Verification and Validation testing" and "Design Verification & Validation activities." The ICS Dizcovery system "functions by processing the binocular camera data collection. The collection of eye movement data is analysed to eye movement in respect to various stimuli throughout testing." However, the results (e.g., specific metrics for eye movement analysis accuracy) of this standalone algorithm performance are not detailed beyond a general statement of compliance and meeting acceptance criteria.

7. The Type of Ground Truth Used

The document does not explicitly detail the type of ground truth used for specific tests. For the overall validation, it implicitly relies on established engineering and safety standards (e.g., IEC, ANSI) as the "ground truth" against which the device's performance is measured. The "Design Verification & Validation activities" would have involved testing against predefined specifications.

8. The Sample Size for the Training Set

This information is not provided in the document. The text indicates that the device has "software" that processes and analyzes data, implying an algorithm that might have been trained, but no details on training data are given.

9. How the Ground Truth for the Training Set Was Established

This information is not provided in the document.

Summary

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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is a blue square with the letters FDA in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.

February 14, 2025

Natus Medical Denmark Aps Therese Coffey Senior Regulatory Affairs Specialist Hoerskaetten 9 Taastrup, DK-2630 Denmark

Re: K242198

Trade/Device Name: ICS Dizcovery (1091) Regulation Number: 21 CFR 882.1460 Regulation Name: Nystagmograph Regulatory Class: Class II Product Code: GWN Dated: July 25, 2024 Received: July 26, 2024

Dear Therese Coffey:

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 (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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.

Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device"

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(https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).

Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review. the OS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).

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 of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.

All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rue"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-device-advicecomprehensive-regulatory-assistance/unique-device-identification-system-udi-system.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.

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For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).

Sincerely,

Shuchen Peng -S

Shu-Chen Peng, Ph.D. Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT, and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health

Enclosure

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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

Indications for Use

Submission Number (if known)

K242198

Device Name

ICS Dizcovery (1091)

Indications for Use (Describe)

ICS Dizcovery is used in the assessment of the vestibular-ocularreflex (VOR) and nystagmus by measuring, recording, displaying, and analyzing eye and head movements.

The intended patient population are children in the age of 10 to 18 and adults in age range from 18 to 99 years with a complaint of dizziness, balance disorder, or vestibular disease.

Type of Use (Select one or both, as applicable)

X Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

CONTINUE ON A SEPARATE PAGE IF NEEDED.

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ICS® Dizcovery™ 510(k) Summary 510(k) Number: K242198

Natus Medical Incorporated | natus.com

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natus.

ICS Dizcovery 510(k): K242198

510K Summary

510(k) Number: K242198

Date: 14 February 2025

Submitted By: Natus Medical Denmark Aps Hoerskaetten 9, 2630 Taastrup, Denmark
Therese Coffey Contact Person: Senior Regulatory Affairs Specialist Natus Medical Incorporated Tel: +353 (0)91 647400 Fax: +353 (0)91 630050 E-mail: Therese.coffey(@natus.com

Proprietary Name: ICS Dizcovery Common Name: Nystagmograph Regulation Number: 21CFR882.1460 Classification Name: Nystagmograph Product code: GWN Device Class: II Predicate Device: ICS Impulse 510(k) number: K151504

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DEVICE DESCRIPTION:

The ICS Dizcovery system is made up of the following components:

A pair of binocular video goggles for testing, controlled through the Otosuite Vestibular PC software
Otosuite Vestibular PC software for controlling tests, displaying test data for the various ● tests, reviewing, and printing test results, as well as and managing patients and patient data, users, and test devices.
A set of Shadeshift® Vision Denied panels; these panels deny the patients vision throughout ● testing whilst allowing the clinician to continue tracking the eyes in darkness. Vision denied testing is needed throughout the test workflow.
. A set of LCD panels; these automatically shift between dark states to facilitate a userfriendly approach to Skew Deviation testing. This removes the need for manually denying vision of each eye separately with the use of a hand or a paddle.
A face cushion which inserts into the goggle frame to promote comfort whilst wearing and allow a better fit to face.

Principals of Operation

The ICS Dizcovery system utilizes the following main components and accessories at minimum to achieve its intended use:

Goggles
Shadeshift® Vision Denied Panels/ LCD Panels
Face Cushion

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ICS Dizcovery 510(k): K242198

Otosuite Vestibular PC software
Other accessories available for use with the ICS Dizcovery include:
Cable Clip ●
USB Cable Service Kit
Head Strap Service Kit ●
Hot Mirror Service Kit ●
Fixation dots
Optical Cleaning Cloth .
Cradle ●
Carrying Case

The system includes goggles connected to a PC with application software through a USB cable. The patient wears the goggles for testing, the goggles are designed to ensure that they can be secured tightly to the patient's head during testing via a head strap, to prevent them from moving or falling off. A face cushion inserts into the goggle frame so that there is a comfortable fit to the face of the patient and prevention of light from leaking in when testing a patient in vision denied status. The cable connecting to the USB port in the PC has a cable clip to secure to the patient's clothing, this prevents the cable tugging or pulling throughout testing. The patient is presented with a stimulus on a surface (such as a wall) this is projected from the goggles. The patient is asked to track the stimuli with their eyes without moving the head. The goggles have light emitting diodes to light up the eyes and Binocular cameras to record the eye movements. Sliding panels can seal off the patient's eyes from the ambient light when the test requires a darkened environment. An additional set of LCD panels assist in a test that requires movement between dark and light in a short timeframe. These are automatic and driven by the software. The Software will collect the eye movement data in respect to the stimuli generated and analyse the data. A credentialled physician will use this data to make a diagnosis. The device and software include a carry case for mobility and an optional cradle to park the goggles when not in use or between tests.

The ICS Dizcovery system is a non-sterile device intended to be used multiple times per day by the clinician, each appointment would require one use per patient in the above-mentioned clinical environment.

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Image /page/8/Picture/0 description: The image shows the word "natus" in a teal color. The font is sans-serif and the letters are rounded. There is a registered trademark symbol after the "s".

Image /page/8/Picture/2 description: The image shows a pair of gray virtual reality glasses with a head strap. The glasses have two lenses and a nose piece. There are two additional lenses that are attached to the sides of the glasses. The glasses are designed to be worn on the head and provide a virtual reality experience.

Figure 1 1091 ICS Dizcovery Goggles (for illustration only)

INDICATIONS FOR USE

ICS Dizcovery is used in the assessment of the vestibular-ocular reflex (VOR) and nystagmus by measuring, recording, displaying, and analyzing eye and head movements.

The intended patient population are children in the age of 10 to 18 and adults in age range from 18 to 99 years with a complaint of dizziness, balance disorder or vestibular disease.

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COMPARISON OF TECHNOLOGICAL CHARACTERISITICS WITH THE PREDICATE DEVICE

Both the subject and predicate device operate on the same technological principle: A wearable measurement system in the form of goggles, with built-in camera and motion sensors that simultaneously track eye- and head movement, respectively. The device connects to a computer with Otosuite Vestibular software that analyzes and compares head and eye movement, to assess the vestibulo-ocular reflex, which is an indicator of overall vestibular function. The software functions by automatically detecting the pupil and tracking its horizontal and vertical movement throughout testing.

Specific design changes in the ICS Dizcovery system include the following:

. Replacement of the camera module with two camera modules with better resolution
Replacement of the static laser module with a movable laser module (freedom laser®) ●
Replacement of the Vision Denied cups with Shadeshift® vision denied panels (same functionality, but improved usability)
Introduction of LCD panels (Improve usability of Skew deviation test) ●
Introduction of an onsite serviceable product- replaceable USB cable, Hot Mirror and Head ● strap (same functionality, improved customer satisfaction)

ICS Dizcovery is similar to the predicate device ICS Impulse in that they both:

Have the same intended use & indications for use
Have the same clinical users ●
Use the same operating principle
Have the same software

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natus.

ICS Dizcovery 510(k): K242198

SUBSTANTIAL EQUIVALENCE TABLE

Specification/Feature	SUBJECT DEVICE:ICS Dizcovery	PREDICATE DEVICE:ICS Impulse (K151504)	Equivalency(Similarities orDifferences)
General
Indications foruse	ICS Dizcovery is used in theassessment of the vestibular-ocularreflex (VOR) and nystagmus bymeasuring, recording, displaying,and analyzing eye and headmovements.The 1091 ICS Dizcovery is used inthe assessment of patients withcomplaints of a vestibular naturesuch as dizziness, disequilibrium,and vertigo. The ICS Dizcoverytype 1091 does not treat ordiagnose the patient; the diagnosisis determined by the credentialedphysician.ICS Dizcovery system is intendedto be used by qualified medicalpersonnel. Typical device users areNeurologists, Ears, Nose, andThroat specialists (ENTs),Audiologists, Physical Therapists,and Technicians supervised by oneof the four mentioned typical users.Professionals with knowledge ofdiagnosing balance disorders. Usersare assumed to have priorknowledge of the medical andscientific facts underlying theprocedures offered by the ICSDizcovery system.The intended patient population arechildren in the age of 10 to 18 andadults in age range from 18 to 99years with a complaint of dizziness,balance disorder or vestibulardisorder.	ICS Impulse is used in theassessment of the vestibular-ocularreflex (VOR) and nystagmusby measuring, recording, displaying,and analyzing eye and headmovements.	Same- theindication foruse statement isexpanded toclarify theintended use, theintended usersand patientpopulaton of thedevice. Theadditionalstatement givesclarity to thegeneral use ofthe device.
Specification/Feature	SUBJECT DEVICE:ICS Dizcovery	PREDICATE DEVICE:ICS Impulse (K151504)	Equivalency(Similarities orDifferences)
Patientpopulation	The intended patient population arechildren in the age of 10 to 18 andadults in age range from 18 to 99years with a complaint of dizziness,balance disorder, or vestibulardisease.	Patient population are children andadults in age range from 10 years to99 years.	Similar-Clarificationadded forpatients with acomplaint ofdizziness.balancedisorder, orvestibulardisease.
Anatomicalsites	The video goggles are placed on thepatient's head.	The video goggles are placed on thepatient's head.	Same
Intended Users	Neurologists, Ears, Nose, andThroat specialists (ENTs),Audiologists, Physical Therapists,and Technicians supervised by oneof the four mentioned typical users.Professionals with knowledge ofdiagnosing balance disorders.	Neurologists and Ears, Nose, andThroat specialists (ENTs),Audiologists, Physical Therapists andTechnicians. Professionals withknowledge of diagnosing balancedisorders.	Same
Where used	Hospitals,ENT/Neurology/Audiology Clinics	Hospitals,ENT/Neurology/Audiology Clinics	Same
User interface	PC software	PC software	Same
Interface	USB 3.0 to PC type A	USB 3.0 to PC, type A	Same
Systemarchitecture	Wearable measurement system inthe form of goggle connecteddirectly to a PC	Wearable measurement system in theform of goggle connected directly toa PC	Same
Technological Characteristics
Single useFace cushion	ICS Dizcovery has a single use facecushion to secure a proper interfacebetween the goggle and the patients	ICS Impulse has a single use facecushion to secure a proper interfacebetween the goggle and the patients	Similar - samefunctionality.
Specification/Feature	SUBJECT DEVICE:ICS Dizcovery	PREDICATE DEVICE:ICS Impulse (K151504)	Equivalency(Similarities orDifferences)
Power supply	Device is powered through USB (5 V DC, 900 mA)	Device is powered through USB (5 V DC, 500mA)	Similar- See substantial equivalence discussion
Camerasystem	Number of sensors: 2Resolution: 1280 x1024 pixels	Number of sensors: 1Resolution: 320 x 240 pixels	Similar- See substantial equivalence discussion
DataManagement	Saved in the PC SW	Saved in the PC SW	Same
Report	The user can generate report from the PC SW	The user can generate report from the PC SW	Same
Specific Technological Characteristics
Eye recording	Simultaneous and individual recording of both left and right eye	Recording of only right eye	Similar- See substantial equivalence discussion
Eye rangetracked	± 30° Horizontal;± 25° Vertical	± 30° Horizontal;± 25° Vertical	Same
Oculomotorstimuli	Static and Moving Laser projection from inside the goggle	Static Laser projection from inside the goggle.	Similar- See substantial equivalence discussion
StimuliViewingDistance	Stimuli presented at 1 to 2 meters from the goggle.	Stimuli presented at 1 to 2 meters from the goggle.	Same
Standards met
AppliedStandards	All relevant Electrical Safety and Biocompatibility standards	All relevant Electrical Safety and Biocompatibility standards	Same(see below for a detailed list of applied standards)

Natus Medical Incorporated | natus.com

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natus.

ICS Dizcovery 510(k): K242198

SUBSTANTIAL EQUIVALENCE DISCUSSION:

The subject device has the same intended use, indications for use, clinical users & operating principle as the predicate device. The products are also similar in terms of technological characteristics as both measure record, display, and analyze eye and head movements.

The ICS Dizcovery system represents an upgrade to the predicate ICS Impulse system hardware to improve usability and capability. The ICS Dizcovery system incorporates binocular and monocular video recording and playback, alongside an in-built moveable laser (freedom laser®), compared with the predicate device (ICS Impulse) which incorporates monocular video recording and playback, alongside an in-built static laser. While the ICS Impulse (predicate device) has a single camera that measures and records the movement of the right eye only, the ICS Dizcovery (subject device) has two-camera's that measure and record the movement of both left and right eye simultaneously as well as individually, providing a comprehensive assessment of the left eye as well as the right eye. The movable laser (freedom laser®) utilised for the ICS Dizcovery enables improved usability by allowing the clinician to test using a moving stimulus rather than a static stimulus (as utilized in the predicate device ICS Impulse). This upgraded mechanism prevents the need to move the patients head throughout testing.

The ICS Dizcovery system, including accessories was independently tested to applicable biocompatibility, Safety, EMC, ANSI S3.45 2009 (R2019), Usability, and Software lifecycle standards and demonstrate the subject device is as safe and effective as the predicate device. Reliability testing was also conducted on the ICS Dizcovery device and accessories by a third party.

Design Verification & Validation activities were performed on the subject device and all tests were verified to meet the required acceptance criteria. The performance testing demonstrated that the differences in the design and performance of the subject device do not affect the intended use of the device or raise any new questions on safety and effectiveness of the ICS Dizcovery.

In conclusion, ICS Dizcovery is substantially equivalent to the predicate device ICS Impulse with respect to Intended Use, technological characteristics, and non-clinical Performance data.

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PERFORMANCE DATA

The following performance data were provided in support of the substantial equivalence determination.

Biocompatibility testing

The biocompatibility evaluation was conducted according to ISO 10993-1:2018. The following tests were considered applicable:

Cytotoxicity
Sensitization
Irritation

The device and its accessories are classified as limited contact (≤24 hours) contact and contact with Intact skin. No issues were found during biocompatibility testing.

Electrical safety, EMC, and other applied standards

The ICS Dizcovery system was tested to and complies with the following applicable safety, electromagnetic compatibility standards and all other applicable standards:

IEC 60601-1:2005+AMD1:2012+AMD2:2020 (Edition 3.2), Medical electrical equipment . - Part 1: General requirements for basic safety and essential performance
IEC 60601-1-2:2014+AMD1:2020 (Edition 4.1), General requirements for basic safety and . essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
IEC 60601-4-2 Ed. 1.0 (2016), Medical Electrical Equipment Part 4-2: Guidance and ● Interpretation - Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
IEC 60601-1-6:2010+A1:2013+A2:2020 (Edition 3.2), Medical electrical equipment Part . 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability,
IEC 62366-1:2015+ AMD1:2020 (Ed.1.1), Medical devices Application of usability ● engineering to medical devices.
IEC 62304:2006 + A1:2015, Medical Device Software Software Lifecycle processes ●
IEC 60825-1:2014+ISH1:2017+ISH2:2017 (Edition 3.0), Safety of laser products Part 1: ● Equipment classification and requirements
IEC 62471:2006, Photobiological safety of lamps and lamp systems
ANSI S3.45-2009 (Reaffirmed 2019)- American National Standard Procedures for Testing ● Basic Vestibular Function

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Software Verification and Validation Testing

Software Verification and Validation testing were conducted, and Basic Documentation Level was provided as recommended by FDA's Guidance for Industry and Staff 'Content of Premarket Submissions for Device Software Functions'.

Mechanical testing

The ICS Dizcovery successfully underwent mechanical testing to ensure that the performance of the device is not degraded by wear and tear over its useful lifetime. A summary of the conducted testing is provided below:

. ICS Dizcovery goggle stimuli projection system cycling accuracy test
Scratch resistance durability testing of the ICS Dizcovery goggle mirror
ICS Dizcovery goggle head strap pull cycle durability test
ICS Dizcovery goggle USB cable bend and pull cycle durability testing

CONCLUSION

The nonclinical performance data support the safety of the device. The hardware and software verification and validation activities demonstrate that the ICS Dizcovery performs as intended in the specified use conditions. The results of these activities demonstrate that the ICS Dizcovery is as safe & effective as the predicate device, rendering it substantially equivalent.

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Regulation Number and Section

§ 882.1460 Nystagmograph.

(a)
Identification. A nystagmograph is a device used to measure, record, or visually display the involuntary movements (nystagmus) of the eyeball.(b)
Classification. Class II (performance standards).