Who is the manufacturer of MAC 800 Resting ECG Analysis System?

Ge Medical Systems China Co., Ltd. filed the 510(k) submission for MAC 800 Resting ECG Analysis System (K142288).

What is the FDA product code for MAC 800 Resting ECG Analysis System?

DPS. It is classified under 21 CFR 870.2340 as a Class 2 device in the Cardiovascular panel.

What is the regulatory pathway for MAC 800 Resting ECG Analysis System?

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

What are the predicate devices for MAC 800 Resting ECG Analysis System?

MAC 800 Resting ECG Analysis System (K090212); MUSE Cardiology Information System (K110132); 12SL ECG Analysis Program (K060833).

Who can help prepare an FDA 510(k) submission like MAC 800 Resting ECG Analysis 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.

MAC 800 Resting ECG Analysis System

K142288 · Ge Medical Systems China Co., Ltd. · DPS · Dec 3, 2014 · Cardiovascular

Device Facts

Record ID	K142288
Device Name	MAC 800 Resting ECG Analysis System
Applicant	Ge Medical Systems China Co., Ltd.
Product Code	DPS · Cardiovascular
Decision Date	Dec 3, 2014
Decision	SESE
Submission Type	Special
Regulation	21 CFR 870.2340
Device Class	Class 2
Attributes	Pediatric

Intended Use

The MAC 800 is a portable ECG acquisition, analysis and recording system. The MAC 800 is intended to be used under the direct supervision of a licensed healthcare practitioner. The MAC 800 is intended to be used by trained operators in a hospital or medical professional's facility environment as well as used in clinics and physician offices outreach centers to record ECG signals from surface electrodes. The MAC 800 is intended to acquire, analyze, display and record information from adult and pediatric populations. Pediatric population is defined as patients between the ages of 0 and 15 years. The basic system shall provide 2 modes of operation: (1) Resting ECG mode and (2) Arrhythmia mode. The basic systems shall print 3, 6-leads of ECG. The device shall be upgradeable to provide software options such as 12-lead ECG measurement and interpretive analysis. Transmission and reception of ECG data to and from a central ECG cardiovascular information system shall be optional. The arrhythmia detection portion of the MAC 800 is provided to the customer for the convenience of automatic documentation.

Device Story

Portable ECG acquisition/analysis system; records surface ECG signals via electrodes. Inputs: ECG signals; patient demographics via SMS/text keypad (T9) or optional barcode/magnetic card scanner. Processing: Resting ECG and Arrhythmia modes; utilizes 12SL ECG algorithm for measurement/interpretation. Outputs: 7" color display; integrated thermal writer for real-time waveforms/reports; optional external laser printer; digital storage (SD card/internal memory); optional export to FTP/shared directory. Used in hospitals/clinics by trained operators. Healthcare providers review reports for clinical decision-making. Benefits: Portable diagnostic ECG capability; automated documentation; connectivity to central cardiovascular information systems.

Clinical Evidence

No clinical data required. Substantial equivalence supported by bench testing, including module verification, system integration testing, and software validation. Compliance with IEC 60601-1, IEC 60601-2-25, IEC 60601-1-2, IEC 62304, IEC 62366, and ANSI/AAMI EC11 standards.

Technological Characteristics

Portable ECG system; 7" LCD display with LED backlight. Connectivity: USB, Wireless LAN, SD card, Ethernet. Energy: AC/Battery. Software: 12SL ECG analysis algorithm. Standards: IEC 60601-1, IEC 60601-2-25, IEC 60601-1-2, IEC 62304, IEC 62366, ANSI/AAMI EC11.

Indications for Use

Indicated for adult and pediatric (0-15 years) patients for ECG acquisition, analysis, and recording. Used in hospitals, clinics, and physician offices under licensed practitioner supervision. Contraindicated for use as a vital signs monitor, during patient transport, for intra-cardiac application, or as an arrhythmia alarm system.

Regulatory Classification

Identification

An electrocardiograph is a device used to process the electrical signal transmitted through two or more electrocardiograph electrodes and to produce a visual display of the electrical signal produced by the heart.

Predicate Devices

MAC 800 Resting ECG Analysis System (K090212)
MUSE Cardiology Information System (K110132)
12SL ECG Analysis Program (K060833)

Related Devices

K081437 — MAC 1600 ECG ANALYSIS SYSTEM · Ge Medical Systems Information Technologies · Jul 15, 2008
K090212 — MAC 800 RESTING ECG ANALYSIS SYSTEM · Ge Medical Syst. Information Technologies · Feb 19, 2009
K133622 — MAC 2000 ECG ANALYSIS SYSTEM · Wipro GE Healthcare · Jan 23, 2014
K173830 — MAC VU360 Resting ECG Analysis System · Ge Medical Systems Information Technologies, Inc. · Sep 18, 2018
K230834 — CARDIPIA ECG / Model: CARDIPIA400H, CARDIPIA800H · Trismed Co., Ltd. · Nov 21, 2023

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 December 3, 2014 GE Medical Systems China Co., Ltd. Kristin Pabst Regulatory Affairs Manager 9900 West Innovation Dr. Wauwatosa, Wisconsin 53226 Re: K142288 > Trade/Device Name: MAC 800 Resting ECG Analysis System Regulation Number: 21 CFR 870.2340 Regulation Name: Electrocardiograph Regulatory Class: Class II Product Code: DPS Dated: October 31, 2014 Received: November 3, 2014 Dear Kristin Pabst, 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. 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 devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in {1}------------------------------------------------ the quality systems (OS) 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 contact the Division of Industry and Consumer Education 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. 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 http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/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 Industry and Consumer Education 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, Melissa A. Torres -S For Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'GE' in a stylized script, enclosed within a blue circle. The circle has decorative swirls or flourishes around the perimeter, giving it a distinctive and recognizable appearance. 510(k) Number (if known): Device Name: MAC 800 Resting ECG Analysis System Indications for Use: The MAC 800 is a portable ECG acquisition, analysis and recording system. The MAC 800 is intended to be used under the direct supervision of a licensed healthcare practitioner. The MAC 800 is intended to be used by trained operators in a hospital or medical professional's facility environment as well as used in clinics and physician offices outreach centers to record ECG signals from surface electrodes. The MAC 800 is intended to acquire, analyze, display and record information from adult and pediatric populations. Pediatric population is defined as patients between the ages of 0 and 15 years. The basic system shall provide 2 modes of operation: (1) Resting ECG mode and (2) Arrhythmia mode. The basic systems shall print 3, 6-leads of ECG. The device shall be upgradeable to provide software options such as 12-lead ECG measurement and interpretive analysis. Transmission and reception of ECG data to and from a central ECG cardiovascular information system shall be optional. The arrhythmia detection portion of the MAC 800 is provided to the customer for the convenience of automatic documentation. Contraindication: The MAC 800 is not intended for use as a vital signs physiological monitor. The MAC 800 is not intended for use during patient transport. The MAC 800 is not suitable for intra cardiac application. The MAC 800 is not designed to provide alarms for arrhythmia detection. Prescription Use_X__ (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (Part 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) {3}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters "GE" in a stylized script, enclosed within a blue circle. There are decorative flourishes around the edge of the circle, resembling water droplets or stylized leaves. The logo is simple and iconic, representing the well-known multinational corporation. ### 510(k) Summary | | In accordance with 21 CFR 807.92 the following summary of information is provided: | |---------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Date: | August 13, 2014 | | Submitted: | Sun YanLi Regulatory Affairs Manager GE MEDICAL SYSTEMS CHINA CO., LTD. No. 19 Changjiang Road National Hi-Tech Dev. Zone Wuxi, Jiangsu, China 214028 | | Primary Contact Person: | Kristin Pabst Regulatory Affairs Manager GE Medical Systems Information Technologies, Inc. Phone: (414) 721-3104 Fax: (414) 721-3863 E-mail: Kristin.Pabst@ge.com | | Secondary Contact Person: | Douglas Kentz Regulatory Affairs Director GE Medical Systems Information Technologies, Inc. Phone: 414 362-2038 Fax: 414-262-2585 E-mail: Douglas.kentz@ge.com | | Device: Trade Name: | MAC 800 Resting ECG Analysis System | | Common/Usual Name: | Electrocardiograph | | Classification Names: | Electrocardiograph (21 CFR 870.2340 ) | | Product Code: | DPS | | Predicate Device(s): | MAC 800 Resting ECG Analysis System, K090212 MUSE Cardiology Information System K110132 12SL ECG Analysis Program K060833 | | Device Description: | The MAC 800 ECG acquisition, analysis and recording system can print and display multiple leads of ECG data. The MAC 800 will provide, in resting ECG mode, ECG quality information using the hookup advisor. The hookup advisor advises users of poor lead quality based on noise measurement It can be upgraded | {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the logo for General Electric (GE). The logo consists of the letters "GE" written in a stylized script, enclosed within a blue circle. The circle has a white border and is surrounded by four white swirls, two on each side of the circle. to provide options such as ECG measurement and interpretation with 12SL. Transmission and reception of ECG data to and from a central ECG cardiovascular information system is also optional. Multiple QT correction formulas including Bazett, Framingham and Fridericia will be available as a user selectable option. Clinical Trials Data Guard and audit trail options are also available to support electronic record requirements. The MAC 800 delivers multiple leads of ECG on full-size reports and includes an SMS/text message telephone keypad for patient demographics and other data entry with T9 input method, an integrated 7" color display, and an integrated thermal writer. The thermal writer will print real time continuous waveform, alphanumeric data and non-real time reports. The device can print the resting ECG report via the external laser printer including USB laser printer and network laser printer. The device will have optional internal memory and removable storage to store resting ECG records. The device also can export the resting ECG record to SD card/shared directory/FTP server as an optional function. An optional barcode reader and magnetic card scanner to enter patient information is available. The MAC 800 can be used as a portable unit. Intended Use: The MAC 800 is a portable ECG acquisition, analysis and recording system. The MAC 800 is intended to be used under the direct supervision of a licensed healthcare practitioner. The MAC 800 is intended to be used by trained operators in a hospital or medical professional's facility environment as well as used in clinics and physician offices outreach centers to record ECG signals from surface electrodes. The MAC 800 is intended to acquire, analyze, display and record information from adult and pediatric populations. Pediatric population is defined as patients between the ages of 0 and 15 years. The basic system shall provide 2 modes of operation: (1) Resting ECG mode and (2) Arrhythmia mode. The basic systems shall print 3, 6-leads of ECG. The device shall be upgradeable to provide software options such as 12-lead ECG measurement and interpretive analysis. Transmission and reception of ECG data to and from a central ECG cardiovascular information system shall be optional. The arrhythmia detection portion of the MAC 800 is provided to {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in white inside. There are three white swirls around the outside of the circle. The logo is simple and recognizable. the customer for the convenience of automatic documentation. Contraindication: The MAC 800 is not intended for use as a vital signs physiological monitor. The MAC 800 is not intended for use during patient transport. The MAC 800 is not suitable for intra cardiac application. The MAC 800 is not designed to provide alarms for arrhythmia detection. Technology: The proposed MAC 800V2 Resting ECG Analysis System is a system based on the predicate MAC 800V1 (K090212) with improvements to the user experience. > The proposed MAC 800V2 Resting ECG Analysis System uses the same modes of operation including Resting ECG mode and Arrhythmia mode to do different ECG examinations, and uses 12SL ECG algorithm (K060833) to do ECG analysis. The major workflow and User Interface does not change. The proposed MAC 800V2 Resting ECG Analysis System provides identical Resting ECG mode and Arrhythmia mode as the predicate MAC 800V1 (K090212), and uses identical 12SL ECG algorithm (K060833). The proposed MAC 800V2 Resting ECG Analysis System employs the same fundamental scientific technology as the predicate MAC 800V1 (K090212). The MAC 800V2 is nearly identical to the MAC 800V1 system, with the addition of the updates and features described in this submission. The proposed MAC 800V2 Resting ECG Analysis System is as safe and effective as the predicate devices. The following table includes comparison of the main features of the device, and includes the features that are different from the predicate. Additional comparison information can be found in Comparison Matrix in Section 12.1. {6}------------------------------------------------ Image /page/6/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized font in the center. There are decorative swirls around the letters. The blue color is consistent throughout the logo. | Feature/Function | Proposed Device MAC 800 V2 | Predicate Device MAC 800V1 | |------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Intended Use | MAC 800V2 intended use is the same as predicate MAC 800V1 with the exception of addition of expanded description to further clarify the medical professional's facility environment to include clinics, physician offices outreach centers. The main features of the device including (but not limited to) mechanical design, OS, ECG system performance, signal acquisition and input, ECG measurement parameters, arrhythmia features and optional software features are identical with predicate MAC 800V1.. | MAC 800V1 intended use is the same as proposed MAC 800V2 with the exception of MAC 800V2 expanded description to further clarify the medical professional's facility environment to include clinics, physician offices outreach centers. The main features of the device including (but not limited to) mechanical design, OS, ECG system performance, signal acquisition and input, ECG measurement parameters, arrhythmia features and optional software features are identical with proposed MAC 800V2.. | | USB Port | 2 USB ports Supports English: Keyboard, barcode and magnetic card reader, laser printer Supports French German, Italian and Spanish keyboards as well as USB WIFI card. | 2 USB Ports Supports English: Keyboard, barcode and magnetic card reader, laser printer Not available | | Supplies and Accessories | Supplies and accessories same as predicate except: Added a compact trolley Added USB WIFI card | Supplies and accessories same as proposed except: Compact trolley not available USB WIFI card not available | | | 2 ECG electrodes and clips removed due to end of life | | | LCD panel | LED backlight to eliminate Hg for RoHS compliance | CCFL backlight | | Anti-drift system | ADS arrhythmia mode ADS Rest mode | ADS Arrhythmia mode | | Data Transmission routes | Wireless Lan data transmission | Wireless Lan data transmission not available | | | 32 GB SD card. | 2GB SD card | | Communication Protocol | Same communication protocols as predicate except: | Same communication protocols as proposed except: | | | Added GE designed DCP protocol to transfer ECG data. | GE designed DCP protocol to transfer ECG data not available | | Examination Order | Adds support for downloading and managing | No support for downloading and managing examination | | | examination orders from the MUSE system | orders from MUSE system | | Data Export | Adds support to export and auto-export data to a FTP server | No support for export and auto- export data to FTP server | | | 32 GB SD card | 2GB SD card | | Shared directory password/PDF file naming/File | Supports alphanumeric password for shared directory | Supports numeric password for shared directory | | Management | Auto-naming and user configurable naming of PDF files | Auto-naming of PDF files | | | Adds Preview to existing file management functionality for enhanced data security and user convenience. | Preview not available | | Technique of Printout | USB laser printer Network laser printer | USB laser printer | | | Printer minimum memory capacity 8MB | Printer minimum memory capacity 2MB | | Report formats | Same report formats as | Same report formats as | | for Laser Printer | predicate except: | proposed except: | | | Adds 2 new ECG report layouts | 2 new ECG report layouts not available | | | Adds a waveform distance auto-adjust for 12 lead printouts to avoid waveform overlap. | Waveform distance auto-adjust for 12 lead printouts not available | | Service Tool | Ability to test network | Ability to test network | | | connection | connection | | | Ping IP test has been added for service purpose only | Ping IP test not available | | Clinical Trials | 5 pharma setting groups per user request | 1 pharma setting group per user request | | | Pop up message to notify "user ID already exists" when creating a non-unique user ID for clinical trial. | "User ID already exists" pop up message not supported | | Enhanced User experience | Ability to enable/disable automatic addition of leading "o" digits to patient ID entry | Not available | | | Added printing of setup configuration file name in addition to saving and setup | Printing of setup configuration file name not supported. | | | information content in a | Saving and set up information | | | configuration file, | content in a configuration file | | | Ability to configure to synchronized clock when it has network connection to a time server. | Not available | {7}------------------------------------------------ Image /page/7/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized font in the center. There are water droplet shapes surrounding the circle. The logo is simple and recognizable. {8}------------------------------------------------ Image /page/8/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'GE' intertwined in a stylized script, enclosed within a blue circle. The circle is surrounded by a series of curved lines, resembling water droplets or stylized leaves, also in blue. The overall design is simple, clean, and recognizable as the brand identity of General Electric. Determination of Summary of Non-Clinical Tests: Substantial Equivalence: The following quality assurance measures were applied to the development of the system: {9}------------------------------------------------ Image /page/9/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized, cursive font in the center. The letters are also blue, and there are three white swirls around the letters. The logo is simple and recognizable, and it is associated with a well-known company. - Risk Analysis � - Requirements Reviews � - Design Reviews � - Testing on unit level (Module verification) � - Integration testing (System verification) � - Final acceptance testing (Validation) � - Performance testing (Verification) � - Safety testing (Verification) � The MAC 800V2 has been thoroughly tested through verification of specifications and validation, including software validation. Verification of compliance with applicable voluntary standards has also been made to support safe use of the device in its intended environment. The proposed MAC 800V2 and its applications were designed and tested for compliance to the following standards: 1. IEC 60601-1: 2005 + C1: 2006 + C2: 2007 Medical electrical equipment - Part 1: General Requirements for Basic Safety and Essential Performance. 2. IEC 60601-2-25: 2011- Medical electrical equipment, Part 2-25: Particular Requirements for the Basic Safety and Essential Performance of Electrocardiographs. 3. IEC 60601-1-2: 2007-Medical Electrical Equipment Part 1-2: General Requirements for Basic Safety and Essential Performance Collateral Standard: Electromagnetic Compatibility 4. IEC 62304:2006, Medical devices - Medical device software -Software life cycle processes 5. IEC 62366: 2007-Medical devices-Application of usability engineering to medical device 6. ANSI/AAMI EC11: 1991/ (R2007)-Diagnostic Electrocardiographic Devices {10}------------------------------------------------ Image /page/10/Picture/0 description: The image shows the logo for General Electric (GE). The logo consists of the letters "GE" written in a stylized script, enclosed within a blue circle. The circle has a white border and is surrounded by four white swirls, two on each side of the circle. Summary of Clinical Tests: The subject of this premarket submission, the proposed MAC 800V2 did not require clinical studies to support substantial equivalence. #### Conclusion: The design changes made have no effect on the device's ability to acquire and analyze ECG data. GE Medical Systems Information Technologies, Inc. considers the proposed MAC 800V2 to be as safe, as effective, and performance is substantially equivalent to the predicate devices.