← Product Code [DSH](/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/DSH) · K073152 # PC-180 / PRINCE 180 EASY ECG MONITOR (K073152) _Shenzhen Creative Industry Co., Ltd. · DSH · Jan 10, 2008 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/DSH/K073152 ## Device Facts - **Applicant:** Shenzhen Creative Industry Co., Ltd. - **Product Code:** [DSH](/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/DSH.md) - **Decision Date:** Jan 10, 2008 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 870.2800 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular - **Attributes:** 3rd-Party Reviewed ## Indications for Use The device is a handheld, personal electrocardiograph (ECG) unit, which can measure electrical activities of the heart easily and conveniently. It's a single LEAD ECG measuring device for home health care use, which can detect, display and store ECG signal, and if possible, provide average heart rate message after ECG measurement. The users can use it themselves to check their heart condition. It is suitable for the adult users (age 18 or older), who suffers from cardio-vascular diseases, or the adult people who are caring about their heart working conditions during their daily life. This device is not intended for use as a conventional diagnostic tool, but use as a healthcare tool which can provide doctor the recorded data as references. This Device is also not intended for recording and transmission of user's ECG signal simultaneously, and it's not recommended to use with implanted pacemaker. ## Device Story Handheld, single-lead ECG monitor for home or clinical spot-checking; operated by adult users or clinicians. Device captures 30-second ECG records via electrodes placed on chest, leg, or palm. Internal software processes electrical signals to calculate average heart rate and analyze heart rhythm. Results, including ECG waveforms and heart rate, are displayed on an integrated LCD screen and stored for review. Provides data as a reference for physicians; not a diagnostic tool. Benefits include convenient, personal heart condition monitoring. ## Clinical Evidence Bench testing only. Device validated against IEC 60601-1, IEC 60601-1-2, and AAMI EC 38 standards. System verification and validation performed on production-equivalent units. Risk analysis and mitigation applied per 21CFR820 and ISO 13485. ## Technological Characteristics Handheld ECG monitor; 3-electrode sensing; 30-240 bpm range. Powered by two AAA batteries. Integrated LCD display. Software-driven analysis. Complies with IEC 60601-1, IEC 60601-1-2, and AAMI EC 38. ## Regulatory Identification A medical magnetic tape recorder is a device used to record and play back signals from, for example, physiological amplifiers, signal conditioners, or computers. ## Predicate Devices - Omron Portable ECG Monitor Model: HCG-801 ([K060766](/device/K060766.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ # 510(k) Summary of Safety and Effectiveness ### Submitter Shenzhen Creative Industry Co., Ltd. 2/F, Block 3, Nanyou Tian'an Industry Town, Shenzhen, GD, 518054 P. R. China 518054 Fax: +86 755 2643 2832 Tel .: +86 755 2643 3514 E-mail: market@creative-sz.com JAN 10 2008 #### Device Name Trade Name: PC-80 /Prince 180 Easy ECG Monitor Common Name: ECG Monitor Classification Name: Electrocardiograph (21CFR870.2340) Classification: Class II ### Predicate Devices (Legally Marketed Devices) The predicate device for ECG Monitor, Model PC-80 /Prince 180 Easy ECG Monitor series is: #### Omron Healthcare, Inc. Omron Portable ECG Monitor Model: HCG-801 510(K) number: K060766 ### Device Description PC-80 / Prince 180 Easy ECG Monitor is a handheld electrocardiograph unit which can measure, display, and store ECG data by the user. The device can calculate the average heart rate and display the heart rhythm after analysis. Furthermore, it's small, light, and easy to use. A 30-second ECG record is measured and stored in this device. The waveform data and heart rate value can be displayed on LCD screen, and those ECG data records can be reviewed. ### Intended Use The device is a handheld, personal electrocardiograph (ECG) unit, which can measure electrical activities of the heart easily and conveniently. It's a single LEAD ECG monitor for home health care use. The users can use it themselves to check their heart condition. The device can detect average Heart Rate, display ECG waveform, and give some information about heart rhythm. It is suitable for the adult user who suffers from cardio-vascular disease, or adults who care about their heart functions during their daily life. This device is not intended for use as a conventional diagnostic tool, but use as a healthcare tool which can provide a doctor recorded data as a reference. This device is also not intended for recording and transmission of user's ECG signal simultaneously, and it's not recommended for use with an implanted pacemaker. The unit is suitable for personal use at home, not suitable for long term monitoring, but spot-checking or clinical patrol at a medical institution or hospital. {1}------------------------------------------------ ## Summary of Technical Characteristics of the Device Compared to the Predicate Devices (Legally Marketed Devices) The Shenzhen Creative Industry PC-80/Prince 180 Easy ECG Monitor and the Omron ECG Model HCG-801 are used to monitor heart rates via three electrodes. The Omron monitors from 2-200 bpm and the Shenzhen device monitors from 30-240 bpm. Both devices use two AAA batteries and are software driven. Both devices are for use on adults and are for prescriptive use. The Shenzhen device's electrodes can be placed on the chest. leg, and palm; however, the Omron device is to be used on the Chest only. They are similar in weight and operating environments. ## Summary of Performance Testing The Shenzhen Creative Industry Co. LTD PC-80/Prince 180 ECG Easy Monitor has undergone IEC 60601-1, IEC 60601-1-2 and AAMI EC 38 testing validation. PC-80/ Prince 180 ECG Easy Monitor substantially have been tested in accordance with the system V & V plan and summary included with the submission using production equivalent units prior to release to market. A risk analysis identifying potential hazards and documenting mitigation of the hazards have been developed and applied as part of Shenzhen Creative Industry Co., LTD design control procedure. Shenzhen Creative Industry Co., LTD quality system confirms to 21CFR820, MDCAS ISO 13485 certified by ORKI. ### Conclusions As stated above, the Shenzhen Creative Industry Co. LTD PC-80/Prince 180 ECG Easy Monitor is safe and effective, complies with the appropriate medical device standards, and is substantially equivalent to the earlier identified predicate device. - End of Section - {2}------------------------------------------------ Image /page/2/Picture/2 description: The image shows the seal of the Department of Health & Human Services - USA. The seal is circular and contains the department's name around the perimeter. In the center is an abstract symbol that resembles a stylized eagle or bird in flight. JAN 10 2008 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Shenzhen Creative Industry Co., Ltd. c/o Mr. Mark Job Regulatory Technology Services LLC 1394 25th Street NW Buffalo, MN 53313 Re: K073152 Trade/Device Name: Easy ECG Monitor Models PC-80 and Prince 180 Regulation Number: 21 CFR 870.2800 Regulation Name: Medical magnetic tape recorder Regulatory Class: Class II (two) Product Code: DSH Dated: December 18, 2007 Received: December 19, 2007 Dear Mr. Job: 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. {3}------------------------------------------------ Page 2 -Mr. Mark Job 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 Center for Devices and Radiological Health's (CDRH's) Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding postmarket surveillance. please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Postmarket Surveillance at 240-276-3474. For questions regarding the reporting of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at 240-276-3464. 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/cdrl/industry/support/index.html. Sincerely yours, Bzimmernan for Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Indications for Use 510(k) Number (if know): Device Name: Easy ECG Monitor Model Name 1: PC-80 Model Name 2: Prince 180 Shenzhen Creative Industry Co., Ltd. Indications for Use: The device is a handheld, personal electrocardiograph (ECG) unit, which can measure electrical activities of the heart easily and conveniently. It's a single LEAD ECG measuring device for home health care use, which can detect, display and store ECG signal, and if possible, provide average heart rate message after ECG measurement. The users can use it themselves to check their heart condition. It is suitable for the adult users (age 18 or older), who suffers from cardio-vascular diseases, or the adult people who are caring about their heart working conditions during their daily life. This device is not intended for use as a conventional diagnostic tool, but use as a healthcare tool which can provide doctor the recorded data as references. This Device is also not intended for recording and transmission of user's ECG signal simultaneously, and it's not recommended to use with implanted pacemaker. Prescription Use V (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 IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Division of Cardiovascular Devices 510(k) Number K073152 --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/DSH/K073152](https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/DSH/K073152) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com