(14 days)
No
The description details a standard microprocessor-based oscillometric blood pressure monitor. It analyzes pressure changes using a microprocessor but does not mention any AI or ML techniques for data analysis, interpretation, or prediction. The software is described for programming, record-keeping, and display, not for advanced analytical capabilities.
No
The device is used for measuring, storing, and displaying blood pressure and heart rate, which aids in diagnosis and follow-up, but it explicitly states that it "does not make any diagnose" and is not directly used for treatment.
No
The "Intended Use / Indications for Use" section explicitly states, "The system does not make any diagnose, it only measures, stores and displays the information." It is described as an "aid or support for the initial diagnosis," implying it provides data for a diagnosis rather than performing the diagnosis itself.
No
The device description clearly details hardware components like an internal electrical air pump, internal valves, and a cuff, indicating it is not software-only. While software is used for programming, data storage, and display, the core function of blood pressure measurement relies on physical hardware.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. They are used to examine these samples outside of the body.
- Device Function: The ABP-2000 G-3 is a non-invasive blood pressure monitor. It measures blood pressure directly on the patient's body using a cuff and oscillometric technique. It does not analyze samples taken from the body.
- Intended Use: The intended use clearly states it measures blood pressure and heart rate of human beings and records these measurements. It explicitly states "The system does not make any diagnose, it only measures, stores and displays the information."
- Device Description: The description details a physical device that is placed on the patient and uses an air pump and valves to take measurements. There is no mention of analyzing biological samples.
Therefore, the ABP-2000 G-3 falls under the category of a non-invasive medical device used for physiological monitoring, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
It is intended to be used as an aid or support for the initial diagnosis and subsequent treatment's follow-up when it is necessary to measure a patient's blood pressure over a determined period of time. The system does not make any diagnose, it only measures, stores and displays the information. The ABP-2000 G-3 (NIBP) monitor is only intended and 'designed:
- for measuring the systolic, diastolic and mean blood pressure as well as the heart rate of human beings.
- for recording during a predetermined period of time the above mentioned measurements (up to 250 measurements).
- to be used along with the ABP-2000 G-3 software for programming as well as record keeping and display in a graphical or tabular report.
Product codes
DXN
Device Description
The ABP-2000 G-3 is an automated, ambulatory, non-invasive blood pressure (NIBP) monitor microprocessor based. The device uses an oscillometric linear deflation technique to determine blood pressure. A cuff is inflated by an internal electrical air pump, and the deflation process is controlled by two internal valves. During deflation, the arterial blood pressure pulses are sensed by the device by means of cuff pressure changes, which are analyzed by the microprocessor in order to determine the blood pressure. The ABP-2000 G-3 can record patient's blood pressure at different and previously determined intervals as clinically scheduled, or can be activated by pressing the Start/Stop button.
The physician can program the measurement intervals as well as the LCD display (it can be disabled to prevent patient from seeing the readings) and then, the device is placed on the patient at the physician's office and is usually worn for 24 hours. The ABP-2000 G-3 software allows the physician to setup the device, the display and to keep all the records. The information is stored on an internal memory that will register each reading. All the data can be downloaded (via serial cable) into the computer software once the study has ended. The information can be analyzed and presented in either graphical or table format, and printed in either format using the PC software.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The ABP-2000 G-3 has been approved according to the British Hypertension Society's protocol. The device complies with all of the requirements of the AAMI SP-10.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 870.1130 Noninvasive blood pressure measurement system.
(a)
Identification. A noninvasive blood pressure measurement system is a device that provides a signal from which systolic, diastolic, mean, or any combination of the three pressures can be derived through the use of tranducers placed on the surface of the body.(b)
Classification. Class II (performance standards).
0
Page 2 of 2
APR 1 2 2002
510(k) Abbreviated Submission ABP-2000 G-3 Biotrac, Inc. Miami, FL
510(k) SUMMARY Summary of Safety and Effectiveness Abbreviated 510(k) Submission
1.- Submitter Information
| Applicant: | Biotrac. Inc. |
|---|---|
| Address: | 7215 N.W. 46th Street |
| Miami, FL 33166 USA | |
| Telephone Number | (305) 594-7474 |
| Fax Number | (509) 267-2283 |
| Contact Person: | Jaime Guttman |
| Biotrac, Inc. | |
| 7215 NW 46th Street, Miami, FL 33166 | |
| (305) 594-7474 (Phone) | |
| (509) 267-2283 (Fax) | |
| Contact Title: | Director |
2.- Name of Device
Contact e-mail:
| Trade Name: | ABP-2000 G-3 |
|---|---|
| Common Name: | Ambulatory Blood Pressure Monitor |
| Classification name: | 21 CFR 870.1130 Non-Invasive Blood-Pressure |
| Measurement System (DXN). | |
| Class II, Circulatory System Devices Panel (74) |
jaime(@biotracmed.com
3.- Predicate Devices
K012647, Tonoport V, PAR Medizintechnik GmbH. K003004, Oscar 2, SunTech Medical Instruments. K964235, ABPM Mobil-o-Graph Blood Pressure Monitor, I.E.M. GmbH.
The ABP-2000 G-3 is substantially equivalent to these devices.
1
Page 3 of 3
510(k) Abbreviated Submission ABP-2000 G-3 Biotrac, Inc. Miami, FL
Image /page/1/Picture/2 description: The image shows the text "K021029 p2/3". The text appears to be handwritten. The text is black against a white background.
4 .- Device Description
The ABP-2000 G-3 is an automated, ambulatory, non-invasive blood pressure (NIBP) monitor microprocessor based. The device uses an oscillometric linear deflation technique to determine blood pressure. A cuff is inflated by an internal electrical air pump, and the deflation process is controlled by two internal valves. During deflation, the arterial blood pressure pulses are sensed by the device by means of cuff pressure changes, which are analyzed by the microprocessor in order to determine the blood pressure. The ABP-2000 G-3 can record patient's blood pressure at different and previously determined intervals as clinically scheduled, or can be activated by pressing the Start/Stop button.
The physician can program the measurement intervals as well as the LCD display (it can be disabled to prevent patient from seeing the readings) and then, the device is placed on the patient at the physician's office and is usually worn for 24 hours. The ABP-2000 G-3 software allows the physician to setup the device, the display and to keep all the records. The information is stored on an internal memory that will register each reading. All the data can be downloaded (via serial cable) into the computer software once the study has ended. The information can be analyzed and presented in either graphical or table format, and printed in either format using the PC software.
5.- Intended. Use
It is intended to be used as an aid or support for the initial diagnosis and subsequent treatment's follow-up when it is necessary to measure a patient's blood pressure over a determined period of time. The system does not make any diagnose, it only measures, stores and displays the information. The ABP-2000 G-3 (NIBP) monitor is only intended and 'designed:
-
for measuring the systolic, diastolic and mean blood pressure as well as the heart rate of human beings.
-
for recording during a predetermined period of time the above mentioned measurements (up to 250 measurements).
-
to be used along with the ABP-2000 G-3 software for programming as well as record keeping and display in a graphical or tabular report.
6 .- Technology
The ABP-2000 G-3 uses the same functional technology employed by the predicate devices.
7 .- Performance
The ABP-2000 G-3 has been approved according to the British Hypertension Society's protocol. The device complies with all of the requirements of the AAMI SP-10.
2
Page 4 of 4
:
510(k) Abbreviated Submission ABP-2000 G-3 Biotrac, Inc. Miami, FL
K021029 p 3/3
8.- Conclusion
The ABP-2000 G-3 performs as safe and effective as the predicate devices.
3
DEPARTMENT OF HEALTH & HUMAN SERVICES
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
PR 1 2 2002
Biotrac, Inc. c/o Mr. Ned E. Devine, Jr. Entela, Inc. 3033 Madison Avenue SE Grand Rapids, MI 49548
Re: K021029
Trade Name: ABP-2000 G-3 Regulation Number: 21 CFR 870.1130 Regulation Name: Non-Invasive Blood Pressure Measurement System Regulatory Class: Class II (two) Product Code: DXN Dated: February 21, 2002 Received: March 29, 2002
Dear Mr. Devine:
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.
4
Page 2 - Mr. Ned E. Devine, Jr.
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 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4646. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely vours.
Dank Tille
Donna-Bea Tillman, Ph.D. Acting Director Division of Cardiovascular and Respiratory Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
Page 34 of 34
510(k) Abbreviated Submission ABP-2000 G-3 Biotrac, Inc. Miami, FL
Indications for Use Statement
510(k) Number (if known):
Device Name: ABP-2000 G-3 (Non-Invasive Ambulatory Blood Pressure Monitor)
Indications for Use: It is intended to be used as an aid or support for the initial multations for oo. "It is interneent's follow-up when it is necessary to measure a diagnosis and subsequence over a determined period of time. The system does not make any pation a blood probable over and displays the information. The ABP-2000 G-3 (NIBP) monitor is only intended and designed:
(ADI ) monitor is only intentive and mean blood pressure as well as the heart rate of human beings.
- for recording during a predetermined period of time the above mentioned measurements (up to 250 measurements).
(up to 250 measurements):
- to be used along with the ABP-2000 G-3 software for programming as well as record keeping and display in a graphical or tabular report.
(PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
N. Q. Tech
Division of Cardiovascular & Respiratory Devices
510(k) Number K021029
Prescription Use
(Per 21 CFR 801.109)