SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE

K071073 · Ge Medical Systems Information Technologies · MHX · May 11, 2007 · Cardiovascular

Device Facts

• Record ID: K071073
• Device Name: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE
• Applicant: Ge Medical Systems Information Technologies
• Product Code: MHX · Cardiovascular
• Decision Date: May 11, 2007
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 870.1025
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional medical facility, such as hospital, clinic, surgical center or doctor's office. It can be used in multiple areas such as operating room (OR), post anesthesia care unit (PACU), emergency department (ED), chest pain clinic, general intensive care unit (ICU), critical care unit, surgical intensive care unit (SICU), respiratory intensive care unit, coronary care unit (CCU), medical intensive care unit (MICU), pediatric intensive care unit (PICU), or neonatal intensive care unit (NICU). The Patient Data Module (PDM) is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transport patient care episodes. Physiological parameter data acquired by the PDM includes ECG, invasive pressure, non-invasive blood pressure, pulse oximetry, temperature, cardiac output and respiration. This device acquires, processes and stores information for all aforementioned parameters and transmits this information to a transport or bedside central processing unit for viewing and alarm surveillance purposes. The Transport Pro patient monitor is intended for use as part of a transport monitoring system for intra-healthcare facility transport. When used with the Patient Data Module (PDM) or the TRAM acquisition module, this device is intended to provide uninterrupted monitoring of physiologic parameter data for adult, pediatric, and neonatal patients during transport from one area of the healthcare facility to another. Physiological parameter data includes ECG, invasive pressure, non-invasive blood pressure, pulse oximetry, temperature and respiration. Both the PDM and TRAM acquisition module acquire, process and store information for all aforementioned parameters. The Solar 8000i patient monitoring system is a multi-parameter physiological patient monitoring system intended for use on adult, pediatric and neonatal patients. It provides uninterrupted monitoring of physiological patient data. The Solar 8000i patient monitoring system is capable of monitoring and analyzing the following parameters for all patient populations: electrocardiogram, invasive pressure, non-invasive blood pressure, pulse, temperature, cardiac output, respiration, pulse oximetry, venous oxygen saturation, transcutaneous pO2 and pCO2, CO2 and respiratory mechanics. The Solar 8000i patient monitoring system is capable of monitoring the following parameters for adult and pediatric patient populations: anesthetic agent concentrations, O2, impedance cardiography, electroencephalography and bispectral index. The Solar 8000i patient monitoring system interfaces with a variety of third-party peripheral medical devices that support serial and/or analog data outputs. Information from these devices can be displayed, trended and stored in the monitoring system. The Solar 8000i patient monitoring system also provides physiological data over the UNITY NETWORK™.

Device Story

System comprises Patient Data Module (PDM) acquisition device, Transport Pro monitor, and Solar 8000i bedside monitor. PDM acquires, processes, and stores physiological signals (ECG, BP, SpO2, temp, cardiac output, respiration); transmits data to host monitors for real-time display and alarm surveillance. Transport Pro provides ruggedized, portable monitoring during intra-facility transport. Solar 8000i serves as bedside host, integrating data from PDM, TRAM modules, or UNITY network. Clinicians use visual/audible alarms to identify parameter limit violations. System supports third-party peripheral device integration via serial/analog outputs. Benefits include uninterrupted patient monitoring across care settings, facilitating timely clinical intervention.

Clinical Evidence

Bench testing only. Quality assurance measures included risk analysis, requirements and design reviews, subsystem verification, integration testing, final acceptance testing (validation), performance testing, safety testing, and environmental testing.

Technological Characteristics

Multi-parameter physiological monitor. Interfaces with PDM or TRAM acquisition modules. Connectivity via UNITY NETWORK. Supports serial/analog inputs from third-party devices. Parameters: ECG, BP, SpO2, temp, cardiac output, respiration, CO2, anesthetic agents, EEG, bispectral index. Complies with voluntary standards for safety and performance.

Indications for Use

Indicated for adult, pediatric, and neonatal patients requiring continuous physiological monitoring in professional medical facilities (hospitals, clinics, surgical centers, doctor's offices). Parameters include ECG, invasive/non-invasive blood pressure, pulse oximetry, temperature, cardiac output, respiration, CO2, venous oxygen saturation, transcutaneous gases, anesthetic agents, impedance cardiography, EEG, and bispectral index.

Regulatory Classification

Identification

The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

Special Controls

*Classification.* Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Arrhythmia Detector and Alarm” will serve as the special control. See § 870.1 for the availability of this guidance document.

Predicate Devices

• Solar 8000M System (K012467)
• Aware Transport Monitor System (K042642)

Reference Devices

• TRAM Module acquisition device (K053121)

Submission Summary (Full Text)

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MAY 1 1 2007

K071073

510(k) Summary of Safety and Effectiveness

| Date: | April 13, 2007 |
|------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Submitter: | GE Medical Systems Information Technologies<br>8200 West Tower Avenue<br>Milwaukee, WI 53223 USA |
| Contact Person: | Karen M. Lunde<br>Regulatory Affairs Program Manager<br>GE Medical Systems Information Technologies<br>Phone: [phone]<br>Fax: [phone]<br>E-mail: [e-mail] |
| Secondary Contact<br>Person: | Lisa M. Baumhardt<br>Regulatory Affairs Program Manager<br>GE Medical Systems Information Technologies<br>Phone: [phone]<br>Fax: [phone]<br>E-mail: [e-mail] |
| Device Trade Name: | Solar 8000i with Patient Data Module / Transport Pro with Patient<br>Data Module |
| Common /Usual Name: | Physiological Patient Monitor |
| Classification Names: | 21 CFR 870.1025 Physiological Patient Monitor (with arrhythmia<br>detection or alarms) |
| Predicate Devices: | K012467 Solar 8000M System<br>K042642 Aware Transport Monitor System |
| Device Description: | The Patient Data Module can be used with the Solar 8000i in a<br>bedside configuration or with the Transport Pro in a transport<br>configuration. |
| | The Patient Data Module (PDM) acquisition device acquires, measures<br>processes, and stores patient physiological parameters. Patient<br>physiological parameter data acquired by the PDM includes 12-Lead<br>ECG, up to four invasive blood pressures (as options), non-invasive<br>blood pressure, Masimo pulse oximetry or Nellcor pulse oximetry, two<br>temperatures, impedance respiration and cardiac output. |
| | The Transport Pro is a host patient monitor that provides continuous<br>patient monitoring capability when coupled with a compatible<br>acquisition device. The Transport Pro is a lightweight, rugged patient<br>monitor that can be used in a transport environment. The Transport<br>Pro provides a means to view patient parameter information and to<br>alert the clinician of parameter limit violations via visual and audible<br>alarms. The Transport Pro must be coupled with the PDM acquisition |

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device with a PDM dock or the TRAM Module acquisition device (K053121) with a TRAM chute.

The Solar 8000i is a host patient monitor that provides continuous patient monitoring capability when coupled with compatible acquisition devices or when connected to the GEMS-IT UNITY network. The Solar 8000i is used in a bedside patient care environment. Like the Transport Pro host patient monitor, the Solar 8000i can be coupled with either the PDM acquisition device or the TRAM Module acquisition device (K053121). Patient physiologic data may also be received from the GEMS-IT Tram-net network and/or multi-parameter modules, or discrete modules located in a TRAM-rac (remote acquisition) housing.

#### Intended Use:

The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional medical facility, such as hospital, clinic, surgical center or doctor's office. It can be used in multiple areas such as operating room (OR), post anesthesia care unit (PACU), emergency department (ED), chest pain clinic, general intensive care unit ((CU), critical care unit, surgical intensive care unit (SICU), respiratory intensive care unit, coronary care unit (CCU), medical intensive care unit (MICU), pediatric intensive care unit (PICU), or neonatal intensive care unit (NICU).

The Patient Data Module (PDM) is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transport patient care episodes. Physiological parameter data acquired by the PDM includes ECG, invasive pressure, non-invasive blood pressure, pulse oximetry, temperature, cardiac output and respiration. This device acquires, processes and stores information for all aforementioned parameters and transmits this information to a transport or bedside central processing unit for viewing and alarm surveillance purposes.

The Transport Pro patient monitor is intended for use as part of a transport monitoring system for intra-healthcare facility transport. When used with the Patient Data Module (PDM) or the TRAM acquisition module, this device is intended to provide uninterrupted monitoring of physiologic parameter data for adult, pediatric, and neonatal patients during transport from one area of the healthcare facility to another. Physiological parameter data includes ECG, invasive pressure, non-invasive blood pressure, pulse oximetry, temperature and respiration. Both the PDM and TRAM acquisition module acquire, process and store information for all aforementioned parameters.

The Solar 8000i patient monitoring system is a multi-parameter physiological patient monitoring system intended for use on adult. pediatric and neonatal patients. It provides uninterrupted monitoring of physiological patient data. The Solar 8000i patient monitoring system is capable of monitoring and analyzing the following parameters for all patient populations: electrocardiogram, invasive pressure, non-invasive blood pressure, pulse, temperature, cardiac output, respiration, pulse oximetry, venous oxyqen saturation, transcutaneous p02 and pC02, CO2 and respiratory mechanics. The

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Solar 8000i patient monitoring system is capable of monitoring the following parameters for adult and pediatric patient populations: anesthetic agent concentrations, O2, impedance cardiography, electroencephalography and bispectral index. The Solar 8000i patient monitoring system interfaces with a variety of third-party peripheral medical devices that support serial and/or analog data outputs. Information from these devices can be displayed, trended and stored in the monitoring system. The Solar 8000i patient monitoring system also provides physiological data over the UNITY NETWORK™.

### Technology:

The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module employs the same functional scientific technology as its predicate devices.

### Test Summary:

The subject of this 510(k) is a design modification for the Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module. The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module complies with the voluntary standards as detailed in Section 4.2 Specific Standards and Guidance of this submission. The following quality assurance measures were applied to the development of the Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module:

- . Risk Analysis
- . Requirements Reviews
- . Design Reviews
- Subsystem Verification .
- Integration testing (System verification) ●
- . Final acceptance testing (Validation)
- . Performance testing
- Safety testing .
- . Environmental testinq

#### Conclusion:

The results of these measurements demonstrated that the Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is as safe, as effective, and performs as well as the predicate devices.

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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

MAY 1 1 2007

GE Medical Systems Information Technologies c/o Karen M. Lunde Program Manager 200 West Tower Avenue Milwaukee, Wisconsin 53223

Re: K071073

Trade/Device Name: Solar 8000i with Patient Data Module / Transport Pro Patient Module Regulation Number: 21 CFR 870.1025 Regulation Name: Arrhythmia detector and alarm (including ST-segment measurement and alarm) Regulatory Class: Class II Product Code: MHX Dated: April 13, 2007 Received: April 16, 2007

Dear Ms. Lunde:

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 - Ms. Lunde

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.

Bhimima for

Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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071073

# Indications for Use

510(k) Number (if known):

Device Name:

510(k) Nun

Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module

Indications for Use:

The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional medical facility, such as hospital, clinic, surgical center or doctor's office. It can be used in multiple areas such as operating room (OR), post anesthesia care unit (PACU), emergency department (ED), chest pain clinic, general intensive care unit (ICU), critical care unit. surgical intensive care unit (SICU), respiratory intensive care unit, coronary care unit (CCU), medical intensive care unit (MICU), pediatric intensive care unit (PICU), or neonatal intensive care unit (NICU),

The Patient Data Module (PDM) is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transport patient care episodes. Physiological parameter data acquired by the PDM includes ECG, invasive pressure, non-invasive blood pressure, pulse oximetry, temperature, cardiac output and respiration. This device acquires, processes and stores information for all aforementioned parameters and transmits this information to a transport or bedside central processing unit for viewing and alarm surveillance purposes.

The Transport Pro patient monitor is intended for use as part of a transport monitoring system for intra-healthcare facility transport. When used with the Patient Data Module (PDM) or the TRAM acquisition module, this device is intended to provide uninterrupted monitoring of physiologic parameter data for adult, pediatric, and neonatal patients during transport from one area of the healthcare facility to another. Physiological parameter data includes ECG, invasive pressure, noninvasive blood pressure, pulse oximetry, temperature and respiration. Both the PDM and TRAM acquisition module acquire, process and store information for all aforementioned parameters.

The Solar 8000i patient monitoring system is a multi-parameter physiological patient monitoring system intended for use on adult, pediatric and neonatal patients. It provides uninterrupted monitoring of physiological patient data. The Solar 8000i patient monitoring system is capable of monitoring and analyzing the following parameters for all patient populations: electrocardiogram. invasive pressure, non-invasive blood pressure, pulse, temperature, cardiac output, respiration, pulse oximetry, venous oxygen saturation, transcutaneous p02 and respiratory mechanics, The Solar 8000i patient monitoring system is capable of monitoring the following parameters for adult and pediatric patient populations: anesthetic agent concentrations, O2, impedance cardlography, electroencephalography and bispectral index. The Solar 8000i patient monitoring system interfaces with a variety of third-party peripheral medical devices that support serial and/or anglog data outputs. Information from these devices can be displayed, trended and stored in the monitoring system. The Solar 8000i patient monitoring system also provides physiological data over the UNITY NETWORK™

| Prescription Use (Part 21 CFR 801 Subpart D) | X | | |
|----------------------------------------------|--------|---------------------------------------------|--|
| | 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)

Bhmmmma

(Division Sign-Off)

Division of Cardiovascular Devices

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