Who is the manufacturer of UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR?

Impact Instrumentation, Inc. filed the 510(k) submission for UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR (K103318).

What is the FDA product code for UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR?

CBK. It is classified under 21 CFR 868.5895 as a Class 2 device in the Anesthesiology panel.

What is the regulatory pathway for UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR?

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

Who can help prepare an FDA 510(k) submission like UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR?

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.

UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR

K103318 · Impact Instrumentation, Inc. · CBK · Apr 7, 2011 · Anesthesiology

Device Facts

Record ID	K103318
Device Name	UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATOR
Applicant	Impact Instrumentation, Inc.
Product Code	CBK · Anesthesiology
Decision Date	Apr 7, 2011
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 868.5895
Device Class	Class 2
Attributes	Therapeutic, Pediatric

Intended Use

The Model 731EMV+ (EMV+) is indicated for use in the management of infant through adult patients weighing ≥5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventilation. It is appropriate for use in hospitals, outside the hospital, during transport and in austere environments where it may be exposed to rain, dust, rough handling and extremes in temperature and humidity. With an appropriate third-party filter in place, it may be operated in environments where chemical and/or biological toxins are present (see External Filter Use). It is not intended to operate in explosive environments. The EMV+ is intended for use by skilled care providers with knowledge of mechanical ventilation, emergency medical services (EMS) personnel with a basic knowledge of mechanical ventilation and by first responders under the direction of skilled medical care providers.

Device Story

Portable critical care ventilator for hospital, transport, and austere environments; provides continuous positive-pressure ventilation. Inputs include patient respiratory parameters; device transforms inputs via pressure/volume targeting to deliver breaths. Modes include Assist/Control (AC), Synchronized Intermittent Mandatory Ventilation (SIMV), and Continuous Positive Airway Pressure (CPAP). Features include Pressure Support (PS) and Noninvasive Positive Pressure (NPPV) with automatic leak compensation (0-15 L/min). Operated by skilled clinicians, EMS personnel, or first responders. Output is mechanical ventilation support; healthcare providers monitor settings and patient response to manage respiratory failure. Benefits include portable, ruggedized life support in extreme conditions.

Clinical Evidence

No clinical data submitted. Bench testing only.

Technological Characteristics

Portable critical care ventilator. Materials and power systems unchanged from predicate. Sensing/actuation: pressure/volume-targeted ventilation. Connectivity: standalone. Standards: ASTM F1100-90, IEC 60601-1, ISO 9919:2005, Mil-Std-461F, Mil-Std-810F. Software: updated to include SIMV and CPAP modes with leak compensation.

Indications for Use

Indicated for infant through adult patients (≥5 kg) with acute or chronic respiratory failure or requiring resuscitation. Contraindicated for use in explosive environments.

Regulatory Classification

Identification

A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and neonatal ventilators are included in this generic type of device.

Predicate Devices

EMV+ ventilator (K091238)

Related Devices

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K120931 — CRITICAL CARE VENTILATOR · Oricare, Inc. · Jun 6, 2013
K032386 — UNI-VENT MODEL 730AEV (AUTOMATIC EMERGENCY VENTILATOR) · Impact Instrumentation, Inc. · Mar 26, 2004
K111473 — UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR · Impact Instrumentation, Inc. · Feb 16, 2012
K162738 — Puritan Bennett 980 Ventilator System · Covidien · Oct 27, 2017

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows a logo for IMPACT Instrumentation Inc. The logo features the word "IMPACT" in large, bold letters, superimposed over a world map. Above the logo, there is a handwritten number, "K103318". The logo is simple and clean, with a focus on the company name and a global image. APR - 7 2011 27 Fairfield Place, West Caldwell, NJ 07006. P.O Box 508, West Caldwell, NJ 07007-0508 ## 510(k) Summary This 510(k) summary consists of a table with the information required in the 510(k) Summary Checklist from the FDA Guidance document. It also includes the completed checklist with approval signature. | Description of Required Information | Information | |---------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Owner's Name | Leslie H. Sherman (President) | | Address | 27 Fairfield Place, West Caldwell NJ 07006 | | Phone | 973-882-1212 | | Fax | 973-882-4993 | | Contact Person | Susan McNevin Ph.D., CQA/ CQE Quality Engineer | | Date this Summary was prepared | January 4, 2011 | | Trade name of device | Uni-Vent® 731 Series Model EMV+® Portable Critical Care Ventilator | | Common name | ventilator | | Classification name | Continuous Ventilator (21 CFR 868.5895, Product Codes CBK, DQA) | | Legally marketed device – Equivalence Claim | This device has updated software from the Predicate EMV+ ventilator (K091238). This update provides SIMV (Synchronized Intermittent Mandatory Ventilation) and CPAP (Continuous Positive Airway Pressure) modes with ventilator support options of Pressure Support and Leak Compensation. | , ー {1}------------------------------------------------ | Description of Required Information | Information | | | | | | | | | | | | | | | | | |------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--| | Description of the device | MODES OF OPERATION The EMV+ offers a range of modes using both pressure and volume targeting that can be selected to optimally manage the patient. Assist/Control (AC): patient receives either controlled or assisted breaths. When the patient triggers an assisted breath they receive a breath based on either the volume or pressure target. Synchronized Intermittent Mandatory Ventilation (SIMV): patient receives controlled breaths based on the set breathing rate. Spontaneous breaths can be either unsupported or supported using Pressure Support. (The software implementation allows for devices to be configured with and without the SIMV mode feature.) Continuous Positive Airway Pressure (CPAP): patient receives constant positive airway pressure while breathing spontaneously. Spontaneous breaths can be either demand flow or supported using Pressure Support. | | | | | | | | | | | | | | | | | | | ADDITIONAL ADJUNCTS OF OPERATION In addition to Modes of Operation, the EMV+ also provides various adjuncts that can be used to manage the patient. Two adjuncts are Pressure Support (PS) and Noninvasive Positive Pressure (NPPV). The table below shows which adjuncts can be used with which modes. It is possible to use more than one adjunct, if the mode permits. | | | | | | | | | | | | | | | | | | Mode Breath Target Pressure Support (PS) Noninvasive Positive Pressure Ventilation (NPPV) AC V & P No No SIMV V & P Yes No CPAP N/A Yes Yes | | | | | | | | | | | | | | | | | | | | Pressure Support (PS): can be used to assist spontaneous breaths in both SIMV and CPAP modes. Noninvasive Positive Pressure (NPPV): provides flow during the expiratory phase to maintain the baseline pressure (CPAP) in spontaneously breathing patients with a leaking airway or facemask. The amount of leak compensation depends on the leak flow rate during the expiratory period and ranges from 0 to 15 liters/min and is automatically adjusted by the ventilator in order to maintain the CPAP target. | | | | | | | | | | | | | | | | | · . · · - . {2}------------------------------------------------ | Description of Required Information | Information | | | | | | | |----------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|--|--|--|--| | Intended Use of Device | The Intended Use is the same as the Predicate device (K091238): "The Model 731EMV+ (EMV+) is indicated for use in the management of infant through adult patients weighing ≥5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventilation. It is appropriate for use in hospitals, outside the hospital, during transport and in austere environments where it may be exposed to rain, dust, rough handling and extremes in temperature and humidity. With an appropriate third-party filter in place, it may be operated in environments where chemical and/or biological toxins are present (see External Filter Use). It is not intended to operate in explosive environments. The EMV+ is intended for use by skilled care providers with knowledge of mechanical ventilation, emergency medical services (EMS) personnel with a basic knowledge of mechanical ventilation and by first responders under the direction of skilled medical care providers. " | | | | | | | | Comparison Technological Characteristics to Predicate | The changes modify the specification of the device in the following manner: EMV+ (K091238) Modified EMV+ Operating Mode: AC Operating Mode: AC, SIMV, CPAP with and without Pressure support and with and without Noninvasive Positive Pressure Ventilation (NPPV) PEEP: 0 to 25 cm H2O PEEP: 0 to 25 cm H2O (The minimum PEEP in CPAP-NPPV is 3 cm H20) There is no change to the product materials or biocompatibility. There is no change to the power input or battery usage. There is no change to Impact®'s intended use statement. There is no change to the devices' fundamental scientific technology. The operating principals remain the same. The modified EMV+ provides the operator methods consistent with the standard of care for managing patients with acute or chronic respiratory failure. | | | | | | | : . . {3}------------------------------------------------ | Description of Required Information | Information | | | | | | | | | | | | | | | |---------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|--|--|--|--|--|--|--|--|--|--|--|--| | Non-Clinical Performance data | This device meets the same performance criteria as the Predicate (K091238). These criteria are specified by: | | | | | | | | | | | | | | | | | Standard Standard Title ASTM F1100-90 Ventilators Intended for use in Critical Care IEC 60601-1 Medical Electrical Equipment - Part 1, General Requirements for Safety ISO 9919:2005 Medical electrical equipment- particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use Additional Environmental Standards: Mil-Std-461F Requirements for the Control of Electromagnetic Interference Characteristics of Subsystems and Equipment Mil-Std-810F Environmental Engineering Considerations and Laboratory Tests | | | | | | | | | | | | | | | | Clinical Performance | N/A. No clinical performance data is being submitted. | | | | | | | | | | | | | | | | Safe and Effective as Predicate | The device design and development process is the same as the Predicate (K091238). It was in accordance with: | | | | | | | | | | | | | | | | | ISO 13485 Quality Systems - Medical Devices ISO 14971 Medical Devices - Application of Risk Management to Medical Devices | | | | | | | | | | | | | | | | | The resulting device being submitted is as safe and effective as the Predicate (K091238). | | | | | | | | | | | | | | | | Other Information requested by FDA | Impact Instrumentation, Inc. will provide the FDA with any additional required information. | | | | | | | | | | | | | | | . : {4}------------------------------------------------ Image /page/4/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo features a stylized eagle with its wings spread, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged in a circular pattern around the eagle. The logo is black and white. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring. MD 20993-0002 Susan McNevin. Ph.D Quality Engineer Impact Instrumentation, Incorporated 27 Fairfield Place West Caldwell, New Jersey 07006 ## APR - 7 2011 Re: K103318 Trade/Device Name: Uni-Vent®) 731 Series Model EMV4® Portable Critical Care Ventilator Regulation Number: 21 CFR 868.5895 Regulation Name: Continuous Ventilator Regulatory Class: II Product Code: CBK and DQA Dated: March 30, 2011 Received: March 31, 2011 Dear Dr. McNevin: 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. {5}------------------------------------------------ Page 2 - Dr. McNevin 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. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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 go to http://www.fda.gov/MedicalDevices/Safety/ReportalProblem/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 Small Manufacturers, International and Consumer Assistance 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 yours, Wh for Anthony Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ ## Indications for Use 510(k) Number (if known): Device Name: Uni-Vent®) 731 Series Model EMV+® Portable Critical Care Ventilator Indications For Use: The Model 731EMV+ (EMV+) is indicated for use in the management of infant through adult patients weighing ≥5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventilation. It is appropriate for use in hospitals, outside the hospital, during transport and in austere environments where it may be exposed to rain, dust, rough handling and extremes in temperature and humidity. With an appropriate third-party filter in place, it may be operated in environments where chemical and/or biological toxins are present (see External Filter Use). It is not intended to operate in explosive environments. The EMV+ is intended for use by skilled care providers with knowledge of mechanical ventilation, emergency medical services (EMS) personnel with a basic knowledge of mechanical ventilation and by first responders under the direction of skilled medical care providers. Prescription Use AND/OR Over-The-Counter Use (Part 21 CFR 801 Subpart D) (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) L. Schultheis (Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control and Dental Devices \$10(k) Number: 103318