NEWPORT E360 VENTILATOR

K053502 · Newport Medical Instruments, Inc. · CBK · Jan 10, 2006 · Anesthesiology

Device Facts

• Record ID: K053502
• Device Name: NEWPORT E360 VENTILATOR
• Applicant: Newport Medical Instruments, Inc.
• Product Code: CBK · Anesthesiology
• Decision Date: Jan 10, 2006
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 868.5895
• Device Class: Class 2
• Attributes: Therapeutic, Pediatric

Intended Use

The e360 Ventilator is intended to provide continuous (ET tube) or non-continuous (mask) ventilatory support and monitoring for infant, pediatric, and adult patients with a tidal volume of ≥ 20 mL. The device is prescription use only. The intended environments include hospital, hospital-type, and intra-hospital transport environments. Hospital use typically includes general care floors, operating rooms, special procedure areas, and intensive and critical care areas within the hospital. Hospital-type use includes facilities such as or similar to surgicenters, sub-acute centers, and special nursing facilities outside of the hospital. Intra-hospital transport includes patient transport within the hospital or hospital-type facility.

Device Story

Newport e360 Ventilator is a pneumatically powered, microprocessor-controlled device providing continuous (ET tube) or non-continuous (mask) ventilatory support. It supports infant, pediatric, and adult patients (tidal volume ≥ 20 mL). Operators use front panel controls to select ventilation modes (A/CMV, SIMV, SPONT) and breath types (volume control, pressure control, volume target pressure control). The device includes a comprehensive alarm system for technical and patient-related safety limits. Used in hospitals (OR, ICU, general care), sub-acute centers, and during intra-hospital transport. It features an internal battery providing ~45 minutes of power. Healthcare providers use the device to manage patient respiration; output includes monitoring data and alarm notifications to assist in clinical decision-making and patient stabilization.

Clinical Evidence

Bench testing only. Comprehensive verification and validation testing performed, including hardware, software, electrical safety, functional safety, EMC, packaging, and environmental testing. All results met pre-defined acceptance criteria.

Technological Characteristics

Pneumatically powered, microprocessor-controlled ventilator. Supports infant/pediatric (≥20 mL) to adult patients. Modes: A/CMV, SIMV, SPONT. Breath types: volume control, pressure control, volume target pressure control. Internal battery (approx. 45 min). Alarms compliant with FDA Draft Reviewer Guidance for Ventilators (1995).

Indications for Use

Indicated for infant, pediatric, and adult patients requiring ventilatory support and monitoring with tidal volumes ≥ 20 mL. Prescription use only.

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

• Newport e500 Ventilator (K030780)

Submission Summary (Full Text)

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### JAN 1 0 2006

K053502

## ATTACHMENT 4, page 162 510(k) SUMMARY

#### A. Sponsor

Newport Medical Instruments, Inc. 1620 Sunflower Ave Costa Mesa, California 92626 Telephone: [phone] Fax: [phone] Contact Person: Richard Waters Vice President, Regulatory Affairs / Quality Assurance

#### Date Prepared B.

12/15/2005

#### C. Device Name

Trade Name: Newport e360 Ventilator

Classification Name: Continuous Use Ventilator

#### D. Device Description

The Newport e360 Ventilator is a pneumatically powered,

microprocessor controlled ventilator. Performance characteristics and clinical features support infant/pediatric (≥20 mL) through adult patients.

Front panel controls allow trained operators to select ventilation controls for volume control, pressure control and volume target pressure control breath types in A/CMV, SIMV and SPONT modes.

A comprehensive alarm system is built- in to alert the user to violations of preset safety limits.

When fully charged, the internal battery provides approximately 45 minutes of power.

The alarms associated with the e360 meet or exceed standards of critical care ventilators and have been developed in compliance with the FDA Draft Reviewer Guidance for Ventilators (1995). The alarms of the e360 span both technical (ventilator related) alarms and non technical alarms (patient related alarms).

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### ATTACHMENT 4, page 163

#### ய் Intended Use

The e360 Ventilator is intended to provide continuous (ET tube) or non-continuous (mask) ventilatory support and monitoring for infant, pediatric, and adult patients with a tidal volume of ≥ 20 mL. The device is prescription use only. The intended environments include hospital, hospital-type, and intra-hospital transport environments. Hospital use typically includes general care floors, operating rooms, special procedure areas, and intensive and critical care areas within the hospital. Hospital-type use includes facilities such as or similar to surgicenters, sub-acute centers, and special nursing facilities outside of the hospital. Intra-hospital transport includes patient transport within the hospital or hospital-type facility.

#### F. Cleared/Predicate Device

Newport e500 Ventilator (K030780).

#### Summary of Substantial Equivalence G.

The Newport e360 Ventilator is substantially equivalent to the cleared/predicate devices in intended use, physical characteristics, performance specifications and safety characteristics.

#### H. Testing

Comprehensive verification and validation testing was performed with the Newport e360 Ventilators including; hardware, software, electrical safety, functional safety, EMC, packaging, and environmental. All test results met pre-defined acceptance criteria.

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Image /page/2/Picture/1 description: The image is a black and white logo for the Department of Health & Human Services - USA. The logo is circular in shape, with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter of the circle. In the center of the circle is a stylized image of an eagle.

Public Health Service

JAN I 0 2006

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

Mr. Richard Waters Vice President, Regulatory Affairs/Quality Assurance Newport Medical Instrument, Incorporated 1620 Sunflower Avenue Costa Mesa, California 92626

Re: K053502

Trade/Device Name: NewPort e360 Ventilator Regulation Number: 868.5895 Regulation Name: Continuous Ventilator Regulatory Class: II Product Code: CBK Dated: December 15, 2005 Received: December 16, 2005

Dear Mr. Waters:

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.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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.

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### Page 2 -Mr. Waters

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); 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.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801). please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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 [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours.

Suptie H. Michien Om-D.

Chiu Lin, Ph.D Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# ATTACHMENT 2, page 160: INDICATIONS FOR USE STATEMENT

510(k) Number (if known):

Device Name: _Newport e360 Ventilator

Indications for Use:

The e360 Ventilator is intended to provide continuous (ET tube) or non-continuous (mask) ventilatory support and monitoring for infant, pediatric, and adult patients with a tidal volume of ≥ 20 mL. The device is prescription use only. The intended environments include hospital, hospital-type, and intra-hospital transport environments. Hospital use typically includes general care floors, operating rooms, special procedure areas, and intensive and critical care areas within the hospital. Hospital-type use includes facilities such as or similar to surgicenters, sub-acute centers, and special nursing facilities outside of the hospital. Intra-hospital transport includes patient transport within the hospital or hospital-type facility

Prescription Use (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 OF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Page 1 of 1

(Posted November 13, 2003)

Suette H. Muchin Omd

n Control, Dental Devices

K053502