← Product Code [JOM](/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/JOM) · K073323 # SA-3000P (K073323) _Medicore Co., Ltd. · JOM · Nov 29, 2007 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/JOM/K073323 ## Device Facts - **Applicant:** Medicore Co., Ltd. - **Product Code:** [JOM](/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/JOM.md) - **Decision Date:** Nov 29, 2007 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 870.2780 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular - **Attributes:** 3rd-Party Reviewed ## Indications for Use The device provides noninvasive measurement of pulse waveform and heart rate by photoelectric plethysmography. The anatomical site for taking the measurement is the left index finger. The device is intended for use with patients age 18 years and older and with a weight of 100 lbs or greater. The device is indicated for use in hospitals, health care clinics and physicians' offices ## Device Story SA3000P is a photoelectric plethysmograph; measures pulse waveform and heart rate via left index finger sensor. Device captures optical signals; processes data to estimate blood flow; displays results for clinician review. Used in hospitals, clinics, and physicians' offices to assist in cardiovascular assessment. Benefits include noninvasive monitoring of physiological parameters. ## Clinical Evidence Bench testing only. No clinical data provided. Device performance was verified against the predicate device to demonstrate substantial equivalence. ## Technological Characteristics Photoelectric plethysmograph; noninvasive optical sensing; intended for left index finger measurement. Class II device (21 CFR 870.2780). ## Regulatory Identification A hydraulic, pneumatic, or photoelectric plethysmograph is a device used to estimate blood flow in a region of the body using hydraulic, pneumatic, or photoelectric measurement techniques. ## Predicate Devices - McPulse by Meridian Co. Ltd. ([K023238](/device/K023238.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}------------------------------------------------ K073323 ## 510(k) Summary Prepared November 23, 2007 | Submitted by: | Medicore Co. Ltd.
4F, Luna B/D, 72 3, Chungdam dong
Gangnam gu
Seoul Korea | |---------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | NOV 2 9 2007 | | Contact Person: | Yoo Byung kuk
Manager
Telephone: | | | 83-2-2056-2650 | | | FAX: | | | 83-2-2056-2688 | | | e-mail: | | | bkyoo@medi-core.com | | Product Name: | SA3000P System | | Common Name: | Pneumatic Plethysmography | | Classification: | JOM; Class II; CFR 21 870.2780 | | Predicate Devices: | McPulse by Meridian Co. Ltd. | | Description of Device: | The device is a photoelectric plethysmograph with is
used to estimate blood flow in a region of the body using
photoelectric measurement techniques | | Intended Use: | The device provides noninvasive measurement of pulse waveform
and heart rate by photoelectric plethysmography. The anatomical
site for taking the measurement is the left index finger. The device
is intended for use with patients age 18 years and older and with a
weight of 100 lbs or greater. The device is indicated for use in
hospitals, health care clinics and physicians' offices | | Comparison with
Predicate Devices: | The SA-3000P is substantially equivalent to the indication for
Use and the technological characteristics of the predicate device,
the Meridian McPulse device (K023238) | {1}------------------------------------------------ Performance: The device has completed performance testing showing that The functions are substantially equivalent to the predicate In addition the device meets the same safety and performance Standards as the predicate. Page 2 of 2 {2}------------------------------------------------ Image /page/2/Picture/2 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 an abstract symbol resembling an eagle or bird in flight, rendered in black. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 ## NOV 2 9 2007 Medicore Co., Ltd c/o Mark Job Responsible Third Party Official Regulatory Technology Services, LLC 1394 25th Street, NW Buffalo, MN 55313 Re: K073323 SA-3000P Regulation Number: 21 CFR 870.2780 Regulation Name: Hydraulic, Pneumatic or Photoelectric Plethysmograph Regulatory Class: Class II (two) Product Code: JOM Dated: November 26, 2007 Received: November 27, 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 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 yours, Blzimuma for Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ 1073323 510(k) Number (if known): Device Name: SA3000P Indications For Use: The device provides noninvasive measurement of pulse waveform and heart rate by photoelectric plethysmography. The anatomical site for taking the measurement is the left index finger. The device is intended for use with patients age 18 years and with a weight of 100 lbs or greater. The device is indicated for use in hospitals, health care clinics and physicians' offices x OR Over-The-Counter Use __ Prescription Use (Per 21CFR 801) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence Of CDRH, Office Of Device Evaluation (ODE) B/Amma --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/JOM/K073323](https://fda.innolitics.com/submissions/CV/subpart-c%E2%80%94cardiovascular-monitoring-devices/JOM/K073323) **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. 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