Who is the manufacturer of ExactVu High Resolution Micro-Ultrasound System?

Exact Imaging, Inc. filed the 510(k) submission for ExactVu High Resolution Micro-Ultrasound System (K192303).

What is the FDA product code for ExactVu High Resolution Micro-Ultrasound System?

IYN. It is classified under 21 CFR 892.1550 as a Class 2 device in the Radiology panel.

What is the regulatory pathway for ExactVu High Resolution Micro-Ultrasound System?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like ExactVu High Resolution Micro-Ultrasound System?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

ExactVu High Resolution Micro-Ultrasound System

Q: What are the predicate devices for ExactVu High Resolution Micro-Ultrasound System?

ExactVu™ High Resolution Micro-Ultrasound System (K190995).

K192303 · Exact Imaging, Inc. · IYN · Oct 1, 2019 · Radiology

Device Facts

Record ID	K192303
Device Name	ExactVu High Resolution Micro-Ultrasound System
Applicant	Exact Imaging, Inc.
Product Code	IYN · Radiology
Decision Date	Oct 1, 2019
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 892.1550
Device Class	Class 2
Attributes	3rd-Party Reviewed

Intended Use

The ExactVu High Resolution Micro-Ultrasound System is intended for use by qualified physicians, physician assistants, sonographers and ultrasound technicians in a healthcare facility for diagnostic ultrasound imaging or fluid flow analysis of the human body in B-Mode (2D), Color Flow Imaging Modes (Color Doppler and Power Doppler) and Combined (B-Mode + CFI Modes). The indications for use are: Small Organ Transrectal Abdominal The system may be used with patients of all ages, but is not designed for pediatric or fetal use. The system is contraindicated for direct cardiac application and for ophthalmic use or any application that causes the acoustic beam to pass through the eye.

Device Story

ExactVu High Resolution Micro-Ultrasound System provides diagnostic ultrasound imaging and guidance for puncture/biopsy. System comprises transducers for signal generation/recording, needle guides, and main unit for data processing and image display. Used by qualified medical professionals in healthcare facilities. Enhancements include workflow improvements (bug fixes, angle reset) and support for transperineal biopsies. Device transforms acoustic data into visual output for clinician review to assist in clinical decision-making and procedural guidance. Benefits include high-resolution imaging for diagnostic and interventional procedures.

Clinical Evidence

No clinical data. Substantial equivalence supported by nonclinical performance testing, including system verification/validation, human factors validation, biocompatibility (ISO 10993-1), sterilization (ISO 11135, ISO 10993-7), electrical safety (IEC 60601-1), electromagnetic compatibility (IEC 60601-1-2), and acoustic output testing (IEC 60601-2-37, IEC 62127-1, IEC 62359).

Technological Characteristics

Diagnostic ultrasound system; B-Mode, Color/Power Doppler. Patient-contacting materials compliant with ISO 10993-1. Sterilization per ISO 11135. Electrical safety per IEC 60601-1; EMC per IEC 60601-1-2. Acoustic output per IEC 60601-2-37, IEC 62127-1, and IEC 62359. Includes transducers, needle guides, and main processing unit.

Indications for Use

Indicated for diagnostic ultrasound imaging or fluid flow analysis (B-Mode, Color/Power Doppler, Combined) in small organ, transrectal, and abdominal applications. Patients of all ages; not for pediatric or fetal use. Contraindicated for direct cardiac or ophthalmic use.

Regulatory Classification

Identification

An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

Predicate Devices

ExactVu™ High Resolution Micro-Ultrasound System (K190995)

Reference Devices

CIVCO Disposable Template Grid (K131161)
CIVCO Poly Ultrasound Transducer Cover (K970513)

Related Devices

K162972 — ExactVu High Resolution Micro-Ultrasound System · Exact Imaging · Dec 2, 2016
K190995 — ExactVu High Resolution Micro-Ultrasound System · Exact Imaging, Inc. · May 10, 2019
K180636 — ExactVu High Resolution Micro-Ultrasound System · Exact Imaging, Inc. · Apr 30, 2018
K143046 — Xario 100, V3.0 · Toshibamedical Systems Corporation · Nov 19, 2014
K160674 — Fujifilm Sonosite Vevo MD Imaging System · FUJIFILM Sonosite, Inc. · Apr 19, 2016

Submission Summary (Full Text)

{0}------------------------------------------------ October 1, 2019 Image /page/0/Picture/1 description: The image shows 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. Exact Imaging, Inc. % Prithul Bom Official Correspondent Regulatory Technology Services, LLC 1000 Westgate Drive. Suite 510k SAINT PAUL MN 55114 Re: K192303 Trade/Device Name: ExactVu™ High Resolution Micro-Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: Class II Product Code: IYN, IYO, ITX, OIJ Dated: September 23, 2019 Received: September 24, 2019 Dear Prithul Bom: 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. 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 located 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. 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 803) for {1}------------------------------------------------ devices or postmarketing safety reporting (21 CFR 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 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. 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 https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. 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. For Thalia T. Mills, Ph.D. Director Division of Radiological Health OHT7: Office of In Vitro Diagnostics and Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) #### K192303 #### Device Name ExactVuTM High Resolution Micro-Ultrasound System Indications for Use (Describe) The ExactVu High Resolution Micro-Ultrasound System is intended for use by qualified physicians, physician assistants, sonographers and ultrasound techniciare facility for diagnostic ultrasound imaging or fluid flow analysis of the human body in B-Mode (2D), Color Flow Imaging Modes (Color Doppler and Power Doppler) and Combined (B-Mode + CFI Modes). The indications for use are: - Small Organ - Transrectal - Abdominal The system may be used with patients of all ages, but is not designed for pediatric or fetal use. The system is contraindicated for direct cardiac application and for ophthalmic use or any application that causes the acoustic beam to pass through the eye. | 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. 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}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the logo for Exact Imaging. The word "EXACT" is in a light green color, with a plus sign in the middle of the "C". Below the word "EXACT" is the word "IMAGING" in a gray color. The logo is simple and modern. Date: 17-July-2019 #### K192303 510(k) Summary This summary of safety and effectiveness is provided as part of this Premarket Notification in compliance with 21 CFR, Part 807, Subpart E, Section 807.92. | Manufacturer: | Exact Imaging, Inc. | |------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------| | Address: | 7676 Woodbine Avenue, Unit 15 Markham, ON L3R 2N2 Canada | | Establishment Registration: | 3012402886 | | Contact Name: | Ms. Sam Rajkumar, MS, RAC, RN | | Title: | Manager, Regulatory Affairs & Quality Assurance | | Phone Number: | +1 905 415 1654 | | Device Proprietary Name: | ExactVu ™ High Resolution Micro- Ultrasound System | | Device Common or Usual Name: | Diagnostic Ultrasound System with Accessories | | Classification Panel: | Radiology | | Product Code: | IYN, IYO, ITX, OIJ | | Regulation Number: | 21 CFR 892.1550, 892.1560, 892.1570 | | Regulation Class: | II | | Regulation Description: | Ultrasonic pulsed echo imaging system, Diagnostic Ultrasound Transducers, Biopsy Needle Guide, Ultrasonic pulsed doppler imaging system | {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the logo for "EXACT Imaging". The word "EXACT" is written in a light green color, with a plus sign in the same color above the "C". Below the word "EXACT", the word "IMAGING" is written in gray. ## Predicate Devices: Substantial equivalence is claimed to the following device: | Trade name | Manufacturer | 510(k) Number | Date Cleared | |---------------------------------------------------------|-----------------------|---------------|--------------| | ExactVu™ High Resolution Micro- Ultrasound System | Exact Imaging Inc. | K190995 | May 10, 2019 | ### Reference Devices: The following reference devices have been used: | Trade name | Manufacturer | 510(k) Number | Date Cleared | |-------------------------------------------|-------------------------------------------|---------------|-----------------------| | CIVCO Disposable Template Grid | CIVCO Medical Instruments Co., Inc. | K131161 | September 17, 2013 | | CIVCO Poly Ultrasound Transducer Cover | CIVCO Medical Instruments Co., Inc. | K970513 | June 20, 1997 | ### Device Description: The ExactVu High Resolution Micro-Ultrasound System is intended for use by qualified medical professionals for diagnostic ultrasound imaging, data processing and guidance of puncture and biopsy. The ExactVu System comprises of transducers responsible for ultrasound signal generation and recording, needle guides and a main unit that controls the transducers, processes the acoustic data, and processes and displays images. ### Intended Use /Indications for use: The ExactVu High Resolution Micro-Ultrasound System is intended for use by qualified physicians, physician assistants, sonographers and ultrasound technicians in a healthcare facility for diagnostic ultrasound imaging or fluid flow analysis of the human body in B-Mode (2D), Color Flow Imaging Modes (Color Doppler and Power Doppler) and Combined (B-Mode + CFI Modes). The indications for use are: - Small Organ - Transrectal ● - Abdominal ● The system may be used with patients of all ages, but is not designed for pediatric or fetal use. The system is contraindicated for direct cardiac application and for ophthalmic use or any application that causes the acoustic beam to pass through the eye. {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows the logo for Exact Imaging. The word "EXACT" is in green, with a plus sign in the middle of the "C". Below the word "EXACT" is the word "IMAGING" in gray. The logo is simple and modern. # Summary of Technological Comparisons: The ExactVu High Resolution Micro-Ultrasound System is an enhanced implementation of the previous FDA-cleared version of ExactVu High Resolution Micro-Ultrasound System. The primary function of both devices is for diagnostic ultrasound imaging, data processing and quidance of puncture and biopsy. The primary difference between ExactVu High Resolution Micro-Ultrasound and the predicate device is enhanced functionality through the introduction of a new accessory and minor workflow improvements. Main advantages compared to the predicate device are: - Minor workflow improvements: bugs fixed and EV29L angle reset. . - Additional support for Transperineal Biopsies. ● There are no known disadvantages. ExactVu High Resolution Micro-Ultrasound System remains substantially unchanged from the predicate with respect to its intended use and performance claims. ### Nonclinical Performance Testing Verification and validation testing have been conducted on the ExactVu High Resolution Micro-Ultrasound system to ensure the safety and effectiveness of the device to perform in accordance to its intended use. The following table provides a summary of the testing performed on the ExactVu High Resolution Micro-Ultrasound. | Type | Activity | Description of Activity | Documentation Results | |---------------------------------------------|-------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | System Verification and Validation | Functional verification of integrated system | Test of ExactVu System and test cases developed to verify system specifications. | The ExactVu System meets all system specifications which is evident through the acceptance of Verification and Validation Results. | | System Verification and Validation | Testing of resolved anomalies | Testing of anomalies present in previously released versions of the device that have been resolved in the ExactVu release. | Previous errors were tested and verified to no longer occur. | | System Verification and Validation | User acceptance testing | Testing of ExactVu System to validate | The ExactVu System meets all usability | | Type | Activity | Description of Activity | Documentation Results | | | | customer needs and intended use. | specifications which is evident through the acceptance of Verification and Validation Results. | | | Human Factors Validation | Testing of critical features by intended users to determine if device is safe and effective for intended users, uses and environments per IEC 62366 and FDA Guidance: "Applying Human Factors and Usability Engineering to Medical Devices". | The ExactVu System compiles with IEC 62366 and FDA Guidance: "Applying Human Factors and Usability Engineering to Medical Devices." | | | System Validation | Product specifications are validated by intended user in a simulated use environment to validate customer needs and intended use. | The ExactVu System meets all product specifications which is evident through the acceptance of Verification and Validation Results. | | | Biocompatibility | Verify that all patient contacting materials are safe for contact with humans through conformance with ISO 10993. | All patient contact materials are biocompatible and comply with ISO 10993-1. | | | Sterilization | Validation of sterilization parameters per ISO 11135 and ISO 10993-7. | All sterilized accessories comply with ISO 11135 and ISO 10993-7. | | | Medical Electrical System Safety | External testing against the requirements of IEC 60601-1 to verify electrical and mechanical safety of the system | The ExactVu System complies with IEC 60601-1. | | Type | Activity | Description of Activity | Documentation Results | | | Electromagnetic Compatibility | External testing against the requirements of IEC 60601-1-2 to verify that the system operates within safe limits of emission and interference requirements. | The ExactVu System complies with IEC 60601-1-2. | | | Acoustic Testing | The acoustic output was measured against requirements of IEC 60601-2-37:2015, IEC 62127-1 :2007, IEC 62359:2010 and Guidance for Industry and Food and Drug Administration Staff: Marketing Clearance of Diagnostic Ultrasound Systems and Transducers issued on June 27, 2019. | The Acoustic Testing for the ExactVu System is performed and reported in compliance with IEC 60601-2-37:2015, IEC 62127-1 :2007, IEC 62359:2010 and Guidance for Industry and Food and Drug Administration Staff: Marketing Clearance of Diagnostic Ultrasound Systems and Transducers issued on June 27, 2019. | {6}------------------------------------------------ Image /page/6/Picture/0 description: The image shows the logo for Exact Imaging. The word "EXACT" is written in green, with a plus sign in the middle of the "C". Below the word "EXACT" is the word "IMAGING" written in gray. {7}------------------------------------------------ Image /page/7/Picture/0 description: The image shows the logo for Exact Imaging. The word "EXACT" is written in green, with a plus sign above the "C". Below the word "EXACT" is the word "IMAGING" written in gray. The logo is simple and modern. ## Clinical Testing This technology is not new; therefore, a clinical study was not considered necessary prior to release. The substantial equivalence of the device is supported by the nonclinical testing. ## Conclusion ExactVu High Resolution Micro-Ultrasound has been shown through comparison and performance testing to be substantially equivalent to the identified predicate device. Any technological differences do not raise new questions of safety and effectiveness.