(97 days)
Not Found
No
The summary describes a standard enteral feeding pump with a graphical user interface and new features for feeding and flushing. There is no mention of AI, ML, image processing, or any data-driven algorithms. The "Mentions AI, DNN, or ML" and "Description of the training set, sample size, data source, and annotation protocol" sections are explicitly marked as "Not Found".
Yes
The device is described as an enteral feeding pump that delivers nutrition, which directly addresses a physiological need (nutrition) and is intended for use in patients with conditions requiring enteral feeding, thus serving a therapeutic purpose.
No
The purpose of this device is to deliver enteral nutrition, not to diagnose a condition. It is an enteral feeding pump.
No
The device description explicitly states the system is comprised of an "enteral feeding pump and disposable Enteral Feeding Sets," which are hardware components.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information about a person's health.
- Device Function: The description clearly states that this device is an enteral feeding pump used to deliver nutrition directly to a patient's gastrointestinal system. It does not analyze any specimens from the body.
- Intended Use: The intended use is for delivering enteral feeding and hydration, not for diagnostic testing.
Therefore, this device falls under the category of a medical device used for treatment/support, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
Intended for use in patients with any condition requiring enteral feeding and/or enteral hydration, which can be accomplished by means of an enteral feeding, pump and pump set. The pump and feeding sets are intended to be used in alternate, acute and home care settings by users ranging from laypersons to clinicians. The purpose of this device is to deliver enteral nutrition at a controlled rate to a patients gastrointestinal system.
Product codes
LZH
Device Description
The ePump "" platform is a new enteral feeding system comprised of an enteral feeding pump and disposable Enteral Feeding Sets. This Class II device is an enteral feeding pump that delivers formula via rotary peristaltic tension loop pumping to provide nutrition for those who do not have the ability to orally ingest food. This enteral feeding pump is an attitude independent pump offering a streamlined graphical user interface that walks the user through the ePump" setup and operation with many new features to allow the ability to both feed nutrition and flush when required.
The ePump™ Enteral Feeding Pump Sets are compatible with standard prefilled formula containers presently available on the market. The ePump" enteral feeding pump sets are also designed to be compatible with present marketed enteral access devices and accessories (extension sets).
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
gastrointestinal system
Indicated Patient Age Range
Not Found
Intended User / Care Setting
alternate, acute and home care settings by users ranging from laypersons to clinicians.
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)
Nonclinical Testing Biocompatibility testing of the proposed device has demonstrated that it meets the requirements of guidelines presented in the 10993 ISO Standard, Part 1, with the FDA modified matrix presented in memorandum G95-1.
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
§ 880.5725 Infusion pump.
(a)
Identification. An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.(b)
Classification. Class II (performance standards).
0
MAY - 5 2004
510(k) Summary
Kendall ePump™ Enteral Feeding Pump and Enteral Feeding Se
In accordance with section 513(1) of the SMDA and as defined in 21 CFR Part 807.3 final rule dated December 14, 1994, this summary is submitted by:
Tvco Healthcare/Kendall 15 Hampshire Street Mansfield, MA 02048 Date Prepared: January 28, 2003
Contact Person 1.
Bridget Gardner Manager, Regulatory Affairs (508)-261-6384
Name of Medical Device 2.
| Classification Name: | Infusion Pump |
|---|---|
| Common or Usual Name: | Enteral Feeding Pump |
| Trade Name: | Kendall ePump TM Enteral Feeding Pump and Enteral Feeding Sets |
3. Identification of Legally Marketed Device
The proposed Kendall ePump " Enteral Feeding Pump and Enteral Feeding Sets is substantially equivalent in intended use, function and mode of operation to the currently marketed Kangaroo 524 Enteral Feeding Pump & Administration Sets (K945964).
Device Description 4 .
The ePump "" platform is a new enteral feeding system comprised of an enteral feeding pump and disposable Enteral Feeding Sets. This Class II device is an enteral feeding pump that delivers formula via rotary peristaltic tension loop pumping to provide nutrition for those who do not have the ability to orally ingest food. This enteral feeding pump is an attitude independent pump offering a streamlined graphical user interface that walks the user through the ePump" setup and operation with many new features to allow the ability to both feed nutrition and flush when required.
The ePump™ Enteral Feeding Pump Sets are compatible with standard prefilled formula containers presently available on the market. The ePump" enteral feeding pump sets are also designed to be compatible with present marketed enteral access devices and accessories (extension sets).
ട്. Device Intended Use
Intended for use in patients with any condition requiring enteral feeding and/or enteral hydration, which can be accomplished by means of an enteral feeding, pump and pump set. The pump and feeding sets are intended to be used in alternate, acute and home care settings by users ranging
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from laypersons to clinicians. The purpose of this device is to deliver enteral nutrition at a controlled rate to a patients gastrointestinal system.
6. Product Comparison
The Kendall ePump™ Enteral Feeding Pump and Enteral Feeding Sets are substantially equivalent in intended use, function and mode of operation to the currently marketed Kangaroo® 524 Enteral Feeding Pump & Administration Sets (K945964).
-
- Nonclinical Testing
Biocompatibility testing of the proposed device has demonstrated that it meets the requirements of guidelines presented in the 10993 ISO Standard, Part 1, with the FDA modified matrix presented in memorandum G95-1.
- Nonclinical Testing
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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes forming its wing. The eagle is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA".
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAY - 5 2004
Ms. Bridget Gardner Manager, Regulatory Affairs Tyco Healthcare/Kendall 15 Hampshire Street Mansfield, Massachusctts 02048
Re: K040196
Trade/Device Name: Kangaroo® ePump™ Enteral Feeding Pump and Enteral Feeding Sets Regulation Number: 880.5725 Regulation Name: Infusion Pump Regulatory Class: II Product Code: LZH Dated: April 27, 2004 Received: April 28, 2004
Dear Ms. Gardner:
We have reviewed your Section 510(k) promarket 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 - Ms. Gardner
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 vour 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 (301) 594-4618. 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 (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
Chiu Lin, Ph.D.
Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known): K040196
Device Name: Kangaroo® ePump" Enteral Feeding Pump and Enteral Feeding Sets
Indications For Use:
Intended for use in patients with any condition requiring enteral feeding and/or enteral hydration, which can be accomplished by means of an enteral feeding, pump and pump set. The pump and feeding sets are intended to be used in alternate, acute and home care settings by users ranging from laypersons to clinicians. The purpose of this device is to deliver enteral nutrition at a controlled rate to a patients gastrointestinal system.
Anton Laing
(Division Sign-Off Division of Anesthesiology, General Hospital, Infection Control, Dental Devices
510(k) Number:
Prescription Use √ (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
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