HEARTSTART MRX MONITOR/DEFIBRILLATOR

{0}------------------------------------------------ #### 8.0 510 (k) Summary summary of 510(k) safety and effectiveness information is This submitted in accordance with the requirements of the Safe Medical Devices Act of 1990 and 21 C.F.R. §807.92. - 1. The submitter of this premarket notification is: 11/4 2 2 2006 Philips Medical Systems This summary was prepared on 1 August 2006 - 2. The name of this device is the HeartStart MRx Monitor/Defibrillator with IntelliVue Networking Software Release 7.01. Classification names are as follows: | Classification | ProCode | Description | |----------------|---------|--------------------------------------------------------------| | 870.2340, II | 74 DPS | Electrocardiograph device | | 870.1130, II | 74 DXN | Non-invasive blood pressure | | 870.2700, II | 74 DQA | Pulse oximeter | | 870.2300, II | 74 MWI | Monitor, Physiological, Patient | | 870.2300, II | 74 MSX | System, Network and Communication,<br>Physiological Monitors | | 868.1400, II | 74 CCK | End-tidal Carbon Dioxide | | 870.5550, II | 74 DRO | External Trascutaneous Pacemaker (Non-<br>invasive) | | 870.5300, II | 74 LDD | Low-energy defibrillator | | 870.1025, III | 74 MKJ | Defibrillators, Automatic, External | | 870.5200, III | 74 LIX | Cardiopulmonary Resuscitation Aid | - 3. The new device is substantially equivalent to the previously cleared HeartStart MRx Monitor/Defibrillator software cleared under K031187 and K051134. - 4. The modification is a change that provides network connectivity via the Philips IntelliVue Network. - 5. The new device has the same Indications for Use as the legally marketed predicate device. - 6. The new device has the same technological characteristics as the legally marketed predicate device. - 7. Verification, validation, and testing activities establish the performance, functionality, and reliability characteristics of the new device with respect to the predicate. Testing involved system level tests, integration tests, environmental tests, and safety testing from hazard analysis. Pass/Fail criteria were based on the specifications cleared for the predicate device and test results showed substantial equivalence. The results demonstrate that web software interface functionality meets all reliability requirements and performance claims. Page {1}------------------------------------------------ Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Philips Medical System c/o Michael J. Doyle Regulatory Affairs Specialist Cardiac and Monitoring Systems 3000 Minuteman Road Andover, Massachusetts 01810-1099 Re: K062233 Trade/Device Name: Heartstart MRx Monitor/Defibrillator Regulation Number: 21 CFR 870.5310 Regulation Name: Automated External Defibrillator Regulatory Class: Class III Product Code: MKJ, LDD, DRO, DPS, DXN, CCK, DQA, MWI, MSX, LIX Dated: October 31, 2006 Received: November 1, 2006 NOV 2 2 2006 Dear Mr Doyle: 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. Iisting 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. {2}------------------------------------------------ Page 2 - Michael J. Doyle Please be advised that FDA's issuance of a substantial equivalence determination docs 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 clectronic 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 (240) 276-0120. 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 (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely vours. Bfimmerman for Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## Indications for Use # 510(k) Number (if known): _ K062233 #### Device Name: HeartStart MRx Monitor/Defibrillator with IntelliVue Networking ## Indications for Use: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician. ### AED Therapy To be used in the presence of a suspected cardiac arrest on patients of at least 8 years of age that are unresponsive, not breathing and pulseless. #### Manual Defibrillation Asynchronous defibrillation is the initial treatment for ventricular fibrillation and ventricular tachycardia in patients that are pulseless and unresponsive. Synchronous defibrillation is indicated for termination of atrial fibrillation. #### Non-invasive External Pacing Therapy The pacing option is intended for treating patients with symptomatic bradycardia. It can also be helpful in patients with asystole, if performed early. #### Pulse Oximetry The SpO2 option is intended for use when it is beneficial to assess a patient's oxygen saturation level. #### Non-invasive Blood Pressure Monitoring The NBP option is intended for non-invasive measurement of a patient's arterial blood pressure. #### End-tidal CO2 The EtCO2 option is intended for non-invasive monitoring of a patient's exhaled carbon dioxide and to provide a respiration rate. #### 12-Lead ECG The 12-Lead ECG function is to provide a conventional diagnostic 12-Lead ECG report, which may include measurements and interpretative statements. #### Q-CPR The Q-CPR™ option provides feedback designed to encourage rescuers to perform resuscitation in accordance with AHA/ERC guidelines for chest compression rate, depth, and duty cycle and ventilation rate, volume and flow rate (inflation time). The Q-CPR option is contraindicated as follows: - The Q-CPR option is contraindicated for use on neonatal and pediatric patients (under 8 years of age or weighing less that 25 kg). - The Q-CPR option is not for use when CPR is contraindicated. | Prescription Use | Yes | |-----------------------------|--------| | (Part 21 CFR 801 Subpart D) | | | | AND/OR | | Over-The-Counter Use | No | | (21 CFR 807 Subpart C) | | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) | Concurrence of CDRH, Office of Device Evaluation (ODE) | |--------------------------------------------------------| |--------------------------------------------------------| (Division Sign-Ui-j Division of Cardiovascular Devices 510(k) Number 166 No Paqe