(22 days)
Not Found
No
The description focuses on the physical components and their function in transmitting ECG signals, with no mention of data analysis or interpretation using AI/ML.
No
The device is intended to transmit electrocardiographic signals, which is for diagnostic purposes, not therapeutic treatment.
No
Explanation: The device is a cable system intended to transmit electrocardiographic signals to ECG monitors. It does not perform interpretation or diagnosis based on the signals.
No
The device description explicitly states that the device includes physical components such as ECG cables, individual leadwires, and accessories, which are hardware.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is to "transmit data in the form of electrocardiographic signals from patient ECG electrode pads to ECG monitors." This describes a device that connects to a patient to acquire physiological signals, not a device used to examine specimens derived from the human body (which is the definition of an IVD).
- Device Description: The description focuses on the physical components (cables, leadwires, connectors), materials, and standards related to patient connection and signal transmission. There is no mention of analyzing biological samples or performing tests on specimens.
- Lack of IVD Characteristics: The document does not mention any of the typical characteristics of an IVD, such as:
- Reagents or assays
- Analysis of biological fluids (blood, urine, etc.)
- Diagnostic testing performed on specimens
The device is clearly intended for in vivo use, meaning it interacts directly with the patient's body to acquire data.
N/A
Intended Use / Indications for Use
The Affinity Cable and Leadwire System is intended transmit data in the form of electrocardiograph signals from patient ECG electrode pads to ECG monitors.
Product codes (comma separated list FDA assigned to the subject device)
74DSA, 74 DRX
Device Description
The Affinity Cable and Leadwire System includes ECG cables, individual leadwires, and accessories. The Affinity Cable and Leadwire System is based upon proven designs to assure secure connections for patient safety and operator ease of use. The Affinity Cable and Leadwire System is reusable and is designed and tested to conform to the following standards: ANSI/AAMI EC53-1995 and 21 CFR Part 898.
The Affinity Cable and Leadwire System is manufactured of materials with a proven history of use for ECG cables. The Affinity Cable and Leadwire System contains no latex or latex products which are external and exposed to the patient.
The Affinity Cable and Leadwire System is provided non-sterile.
The Affinity Cable and Leadwire System is designed to minimize the potential for incorrect attachments. Leadwires are color coded for positive identification. Leadwire connectors include recessed sockets to preclude attachment to power cables or outlets.
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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 870.2900 Patient transducer and electrode cable (including connector).
(a)
Identification. A patient transducer and electrode cable (including connector) is an electrical conductor used to transmit signals from, or power or excitation signals to, patient-connected electrodes or transducers.(b)
Classification. Class II (performance standards).
0
AFFINITY
510(k) Summarv Prepared 3/17/98
MAR 25 1998
-
- Manufacturer: Affinity Medical Technologies, LLC 17332 Von Karman, Suite 115 Irvine, CA 92614 714-477-9495 Contact: Mary F. Phillipp
-
- Trade Name: Affinity Medical Patient Cable Systems Common Name: Patient Cable Icable, transducer and electrode, patient (including connector)]
Classification: Class II 74DSA (CFR 870.2900)
-
- Predicate Device: This device is substantially equivalent to the Tronomate™ Patient Cable and Leadwire System (K952659).
-
- Description: The Affinity Cable and Leadwire System includes ECG cables, individual leadwires, and accessories. The Affinity Cable and Leadwire System is based upon proven designs to assure secure connections for patient safety and operator ease of use. The Affinity Cable and Leadwire System is reusable and is designed and tested to conform to the following standards: ANSI/AAMI EC53-1995 and 21 CFR Part 898.
The Affinity Cable and Leadwire System is manufactured of materials with a proven history of use for ECG cables. The Affinity Cable and Leadwire System contains no latex or latex products which are external and exposed to the patient.
The Affinity Cable and Leadwire System is provided non-sterile.
The Affinity Cable and Leadwire System is designed to minimize the potential for incorrect attachments. Leadwires are color coded for positive identification. Leadwire connectors include recessed sockets to preclude attachment to power cables or outlets.
- ട. Intended Use: The Affinity Cable and Leadwire System is intended transmit data in the form of electrocardiograph signals from patient ECG electrode pads to ECG monitors.
-
-
- Comparison to Predicate Device: This device has the same technological characteristics (i.e., design, material composition) as the Tronomate™ Patient Cable and Leadwire System (K952659). Further, the Affinity Medical Patient Cable Systems are designed and tested in accordance with ANSI/AAMI EC53-1995, ECG Cable and Leadwires.
-
Attachment VII
1
Image /page/1/Picture/1 description: The image shows the logo for the Department of Health & Human Services (HHS). The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" around the perimeter. Inside the circle is an abstract image of an eagle with its wings spread.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAR 2 5 1998
Ms. Mary F. Phillipp Affinity Medical Technologies, LLC 17332 Von Karman, Suite 115 Irvine, CA 92614
Re: K980806 Affinity Medical Patient Cable Systems Regulatory Class: II (two) Product Code: 74 DRX February 27, 1998 Dated: March 3, 1998 Received:
Dear Ms. Phillipp:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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 (Premarket Approval), it may be subject to such additional controls. Existing major requlations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21.CER.Part 820) and that, through periodic (QS) = inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in requlatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
2
Page 2 - Ms. Mary F. Phillipp
This letter will allow you to begin marketing your device as described in your 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 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4648. 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 requlation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours,
Thomas J. Callahan
Thomas J. Callahan, Ph.D. Director Division of Cardiovascular, Respiratory, and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
"Indications For Use" Statement
Unknown 510(k) Number:
Affinity Medical Patient Cable Systems Device Names:
Indications for Use: The Affinity Medical Patient Cable Systems are intended to transmit data in the form of electrocardiographic signals from patient ECG electrode pads to ECG monitors.
(PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NECESSARY)
| Concurrence of CDRH, Office of Device Evaluation (ODE) |
|---|
| -------------------------------------------------------- |
| Prescription Use
| (Per 21 CFR 801.109) | OR | Over-the-counter Use |
|---|---|---|
| ------------------------------------------ | ---- | ---------------------- |
| Optional Format 1-2-96 |
|---|
| ------------------------ |
3/24/98 C. Casey R. W. Saperstein
(Division Sign-Off)
Division of Card and Neurological D 510(k) Number
Attachment I
7