ECG is intended to disclose either normal condition or patterns of arrhythmia, myocardial ischemia, rate abnormalities, or features of prognostic value in patients:

suspected of cardiac abnormalities, or
in populations of patients at an age or period in which a routine baseline evaluation of ECG characteristics are desired.
QT Analysis is useful in the assessment of long QT syndrome (LQTS). In some instances, LQTS can be corrected by pharmacologic therapy. QT analysis is also used to measure QT dispersion, the difference between maximal and minimal QT values. QT dispersion is a measure of the inhomogeneity of ventricular repolarization.
The PCECG-1200 System With MEANS has been tested to measure Heart Rate Variability within 1 millisecond tolerance. The clinical significance of HRV measures should be determined by a physician.
The PCECG-1200 System With MEANS has been tested to measure Late Potential within 1 millisecond tolerance in the time domain, and 1 microvolt tolerance in voltage. The clinical significance of Heart Rate Variability measures should be determined by a physician.

Stress testing intended use:
Angina pectoris (chest pain) is a clinical syndrome resulting from myocardial ischemia, indicative of a reduced blood supply to the cardiac muscle. The electrocardiogram may establish the diagnosis of ischemic heart disease if characteristic changes are present. Stress testing is the most widely used method to decide whether this chest pain is related to myocardial ischemia, and thereby coronary artery disease. In stress testing, the contractile capability of the heart muscle is monitored via ECG during patient exercise. Patients are exercised by bicycle, treadmill, or other means while continuously monitoring the ECG. Exercise loads are determined by predefined protocols. The ECG signals are recorded for the resting, exercise and recovery portions of the exercise protocol. The changes in ECG waveforms are compared to the resting ECG records. Although not necessary, most of the commercial stress test systems control the bicycle or treadmill automatically according to the requirements of the chosen protocol.

ST segment monitoring is intended as an aid in the evaluation of myocardial ischemia in patients with known or suspected coronary artery disease. The ST segment algorithm has been tested for accuracy of the ST segment data, and a database has been used as a tool for performance testing. The significance of the ST segment changes must be determined by a physician.

Device Description

The PCECG-1200 System With Modular ECG Analysis System (MEANS) is designed to disclose either normal condition or patterns of arrhythmia, myocardial ischemia, rate abnormalities, or features of prognostic value. The System comprises:

· Data Acquisition Unit
· RF transceiver
· USB communications cable
· Software application
· Software access security lock (dongle), optional

The system acquires ECG data and displays it on the color monitor, calculates and controls some parameters of ECG display such as sweep speed, filters line interference and muscle noises introduced during monitoring, makes necessary outputs, handles the user interface, and controls the flow of operations.

Acquired data is stored, and subsequently transferred to the PC for display. Up to 12 channels of real time ECG display are possible. The available commands, calculation of results and status messages are also displayed. All commands are initiated via keyboard.

ECG is analyzed by the Modular ECG Analysis System (MEANS), which is a cleared O.E.M. SW Application obtained by Norav from the producer: the Department of Medical Informatics Erasmus University Medical Center Rotterdam, the Netherlands.

AI/ML Overview

The provided document is a 510(k) Summary for the NORAV PCECG-1200 System with Modular ECG Analysis System (MEANS). It outlines the device's intended use, technological characteristics, and substantial equivalence to predicate devices. However, it does not contain the specific details about acceptance criteria or a dedicated study that proves the device meets those criteria in a way that directly maps to your requested table and study information.

Instead, the document makes general statements about testing and performance. It mentions:

"The PCECG-1200 System With MEANS has been tested to measure Heart Rate Variability within 1 millisecond tolerance."
"The PCECG-1200 System With MEANS has been tested to measure Late Potential within 1 millisecond tolerance in the time domain, and 1 microvolt tolerance in voltage."
"The ST segment algorithm has been tested for accuracy of the ST segment data, and a database has been used as a tool for performance testing."

These are statements about what was tested and the reported performance, but they lack the full context of "acceptance criteria" (i.e., the predefined thresholds that must be met for approval) and the detailed methodology of the studies.

Therefore, many of the requested fields cannot be extracted directly from this document.

Here's how I can address your request based on the available information, noting where data is missing:

1. Table of Acceptance Criteria and Reported Device Performance

Feature/Measurement	Acceptance Criteria (Stated or Implied)	Reported Device Performance (Stated or Implied)
Heart Rate Variability	Within 1 millisecond tolerance (implied)	Measures within 1 millisecond tolerance
Late Potential (Time Domain)	Within 1 millisecond tolerance (implied)	Measures within 1 millisecond tolerance
Late Potential (Voltage)	Within 1 microvolt tolerance (implied)	Measures within 1 microvolt tolerance
ST segment algorithm accuracy	Implied satisfactory accuracy *	"Tested for accuracy" and "database used as a tool for performance testing."

Note: The document implicitly suggests these tolerances are "acceptance criteria" because it states the device "has been tested to measure... within" these values. However, it does not explicitly define these as pre-established acceptance criteria that had to be met. For ST segment accuracy, no specific numerical criterion is provided, only that it was "tested for accuracy."

2. Sample size used for the test set and the data provenance

Sample size: Not specified. The document only mentions that a "database has been used as a tool for performance testing" for the ST segment algorithm.
Data provenance: Not specified for any of the performance claims.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

Number of experts: Not specified.
Qualifications of experts: Not specified.

4. Adjudication method for the test set

Not specified.

5. If a multi-reader, multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

No MRMC comparative effectiveness study involving human readers and AI assistance is mentioned in this document. The device is for automated ECG analysis.

6. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done

Yes, the performance claims strongly suggest standalone (algorithm-only) testing as the device is an "ECG Analysis System" intended for automated analysis. For example, "The PCECG-1200 System With MEANS has been tested to measure Heart Rate Variability..." implies testing the algorithm itself.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.)

Not explicitly stated. For Heart Rate Variability and Late Potential, the "tolerance" suggests a comparison against a highly accurate reference measurement or a gold standard method. For the "ST segment algorithm accuracy," it refers generally to a "database," but the nature of the ground truth within that database (e.g., expert annotations, confirmed diagnoses) is not detailed.

8. The sample size for the training set

Not specified. The document states the MEANS software is a "cleared O.E.M. SW Application obtained by Norav from the producer: the Department of Medical Informatics Erasmus University Medical Center Rotterdam, the Netherlands." This implies the training (and development) was done by the OEM.

9. How the ground truth for the training set was established

Not specified. This information would typically reside with the original developer of the MEANS software, not necessarily in this 510(k) submission.

Summary

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Image /page/0/Picture/0 description: The image shows the word "NORAV" in a stylized font, with a heart shape in place of the "O". A line runs beneath the word, resembling an EKG readout. Below the word, the word "medical" is written in a smaller font.

Summary of Safety and Effectiveness

510(k) Summary

Submitter

21 CFR 807 92(c)

21 CFR 807.92(a)(1)

NOV 1 0 2011

lot 3

KI10463

Arazy Group - Medical device Consultatuts Telephone (972) 4-994-7880 Fax number (972) 4-994-4224 Industrial Park 13, M.P. Misgav Mitzpe Aviv 20187 Israel Benny Arazy - CEO and President benny a @mmy a com

Manufacturer

Norav Medical Ltd. 2 Hamada Street, PO Box 81 Yokneam 20692 Israel Telephone (972) 4-9893001 Fax number (972) 4-9893004 Contact: David Seal - QA Manager davidi@nomy.com

Device Name:

PCECG-1200 System With Modular ECG Analysis System (MEANS) 21 CFR 807.92(a)(2)

Trade Name: PCECG-1200 System With MEANS

The classification name 1	monitor, physiological, patient (without arrhythmia detection or alarms)
Regulation Number 1	870.2300
Classification code 1	MWI
The classification name 2	transmitters and receivers, electrocardiograph, telephone
Regulation Number 2	870.2920
Classification code 2	DXH

Substantial Equivalence 21 CFR 807.92(a)(3)

Norav's PC ECG 1200W System K080141 for complete physical and functional identity 1.
Welch Allyn's CardioPerfect Workstation (CPWS) V 1.6.2 Software K032478 (developed by P. 2. Rijnbeek) on the grounds of close similarity

Device Definition 21 CFR 807.92(a)(4)

· Data Acquisition Unit
· RF transceiver
· USB communications cable
· Software application
· Software access security lock (dongle), optional

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Ps. 110463 Ps. 2 of 3

Image /page/1/Picture/1 description: The image shows a logo with the word "NORAV" in a stylized font. The letters are connected by a line that resembles an electrocardiogram (ECG) tracing, with a heart shape incorporated into the "O". Below the word "NORAV", there is some text that is difficult to read due to its small size and image quality. The logo appears to be for a medical or healthcare-related company, given the heart and ECG elements.

Summary of Safety and Effectiveness

Intended Use 21 CFR 807.92(a)(5)

ECG intended use:

ECG is intended to disclose either normal condition or patterns of anthythmia, myocardial ischemia, rate abnormalities, or features of prognostic value in patients:

suspected of cardiac abnormalities, on
in populations of patients at an age or period in which a routine baseline evaluation of ECG characteristics are desired.
QT Analysis is useful in the assessment of long QT syndrome (LQTS). In some instances, LQTS can be corrected by pharmacologic therapy. QT analysis is also used to measure QT dispersion, the difference between maximal and minimal QT values. QT dispersion is a measure of the inhomogeneity of ventricular repolarization.
The PCECG-1200 System With MEANS has been tested to measure Heart Rate Variability within 1 millisecond tolerance. The clinical significance of HRV measures should be determined by a physician.
The PCECG-1200 System With MEANS has been tested to measure Late Potential within 1 millisecond tolerance in the time domain, and 1 microvoilt tolerance in voltage. The clinical significance of Heart Rate Variability measures should be determined by a physician.

Stress testing intended use:

Angina pectoris (chest pain) is a clinical syndrome resulting from myocardial ischemia, indicative of a reduced blood supply to the cardiac muscle. The electrocardiogram may establish the . diagnosis of ischemic heart disease if characteristic changes are present. Stress testing is the most widely used method to decide whether this chest pain is related to myocardial ischemia, and thereby coronary artery disease. In stress testing, the contractile capability of the heart muscle is monitored via ECG during patient exercise. Patients are exercised by bicycle, treadmill, or other means while continuously monitoring the EOG. Exercise loads are determined by predefined protocols. The ECG signals are recorded for the resting, exercise and recovery portions of the exercise protocol. The changes in ECG waveforms are compared to the resting ECG records. Although not necessary, most of the commercial stress test systems control the bicycle or treadmill automatically according to the requirements of the chosen protocol.

Technological characteristics 21 CFR 807.92(a)(6)

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Image /page/2/Picture/1 description: The image shows the word "NORAV" in a stylized font. The "O" in NORAV is shaped like a heart. Below the word "NORAV" is the word "medical" in a smaller font.

Summary of Safety and Effectiveness

Recognized Consensus Standards

IEC 60601-1 Medical Electrical Equipment Part 1: General Requirements for Safety, 1988; Amendment 1, 1991-11, Amendment 2, 1995
IEC 60601-2-25 Amendment 1 (1999), Medical electrical equipment, Part 2: Particular requirements for the safety of electrocardiographs
IEC 60601-2-27 (1994) Medical electrical equipment, Part 2: Particular requirements for the safety of electrocardiographic monitoring equipment

ISO 14971:2007. Medical devices - Application of risk management to medical devices

Summary 21 CFR 807.92(b)(3)

PCECG-1200 System With MEANS System constitutes a safe and reliable medical device. Similarly to the predicate devices, the System operation presents no adverse health effect or safety risks to patients when used as intended.

Name: David Seal

Signature: D. Seal

Position: QA Manager

Date: 18 September 2011

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Image /page/3/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 words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized graphic of an eagle or bird-like figure with three curved lines representing its wings or body. The overall design is simple and conveys a sense of official government authority.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002

NOV 1 0 2011

Norav Medical Ltd. c/o Mr. Benny Arazy Arazy Group - Medical Device Consultants Industrial Park 13, M.P. Misgav Mitzpe Aviv Israel 20197

Re: K110463

Trade/Device Name: PCECG-1200 System With MEANS Regulation Number: 21 CFR 870.2300 Regulation Name: Cardiac Monitor (Including Cardiotachometer and rate alarm) Regulatory Class: Class II (two) Product Code: MWI Dated: September 21, 2011 Received: October 11, 2011

Dear Mr. Arazy:

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.

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Page 2 -- Mr. Benny Arazy

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.fdagov/AboutFDA/CentersOffices/CDRH/CDRHQffices/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/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 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/Resourcesfor You/Industry/default.htm.

Sincerely yours,

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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K110463 pg 1 of 1

Indications for Use

510(k) Number (if known):

Device Name: PCECG-1200 System With MEANS

Indications for Use:

ECG intended use:

ECG is intended to disclose either normal condition or patterns of arrhythmia, myocardial ischemia, rate abnormalities, or features of prognostic value in patients:

suspected of cardiac abnormalities, or
in populations of patients at an age or period in which a routine baseline evaluation of ECG characteristics are desired.
QT Analysis is useful in the assessment of long QT syndrome (LQTS). In some instances, LQTS can be corrected by pharmacologic therapy. QT analysis is also used to measure QT dispersion, the difference between maximal and minimal QT values. QT dispersion is a measure of the inhomogeneity of ventricular repolarization.
The PCECG-1200 System With MEANS has been tested to measure Heart Rate Variability within 1 millisecond tolerance. The clinical significance of HRV measures should be determined by a physician. 5) The PCECG-1200 System With MEANS has been tested to measure Late Potential within 1 millisecond tolerance in the time domain, and 1 microvolt tolerance in voltage. The clinical significance of Heart Rate Variability measures should be determined by a physician.

Stress testing intended use:

Angina pectoris (chest pain) is a clinical syndrome resulting from myocardial ischemia, indicative of a reduced blood supply to the cardiac muscle. The electrocardiogram may establish the diagnosis of ischemic heart disease if characteristic changes are present. Stress testing is the most widely used method to decide whether this chest pain is related to myocardial ischemia, and thereby coronary artery disease. In stress testing, the contractile capability of the heart muscle is monitored via ECG during patient exercise. Patients are exercised by bicycle, treadmill, or other means while continuously monitoring the ECG. Exercise loads are determined by predefined protocols. The ECG signals are recorded for the resting, exercise and recovery portions of the exercise protocol. The changes in ECG waveforms are compared to the resting ECG records. Although not necessary, most of the commercial stress test systems control the bicycle or treadmill automatically according to the requirements of the chosen protocol.

Prescription Use [X]
(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)

	(Division Sign-Off)
	Division of Cardiovascular Devices
510(k) Number	K110463

(Posted November 13, 2003)

Page 1 of 1

Regulation Number and Section

§ 870.2300 Cardiac monitor (including cardiotachometer and rate alarm).

(a)
Identification. A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal produced by an electrocardiograph, vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits.(b)
Classification. Class II (performance standards).