LogoFDA 510(k) Search
K Number
K040114
Device Name
ABBOTT DATA PORT PC, MODEL 12181
Manufacturer
ABBOTT LABORATORIES
Date Cleared
2004-01-29

(9 days)

Product Code
FRN
Regulation Number
880.5725
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Abbott DataPort PC is an optional computer (PC) software accessory for use exclusively with the Abbott Plum A+ and A+3 Infusion Pumps in a biomedical technical service environment. The indications for use are the indications for use of the parent devices belonging to the Abbott Plum A+ Infusion Pump family, which are the Abbott Plum A+ and Abbott Plum A+3 Infusion Pumps. Infusion pumps in the Abbott Plum A+ Infusion Pump Family are used in parenteral, enteral and epidural therapies and the administration of whole blood products. The Abbott Plum A+ and A+3 Infusion Pumps are designed to deliver infusions over a broad range of infusion rates from multiple container types.
Device Description
The Abbott DataPort PC software supports data transfer between a single computer (PC) and up to 15 Abbott Plum A+ Infusion Pumps, or up to 4 Abbott Plum A 13 Infusion Pumps. Abbott DataPort PC allows authorized users to retrieve infuser alarm logs, event history logs, and biomedical settings from interfaced infusers, and to edit and send modified biomedical settings to the interfaced infusers from the PC.
More Information

K024084, K021350, K011442, K982159

Not Found

No
The summary describes software for data transfer and configuration of infusion pumps, with no mention of AI/ML terms, image processing, or performance metrics typically associated with AI/ML models.

No.
The document states that the Abbott DataPort PC is an optional computer software accessory for use exclusively with the Abbott Plum A+ and A+3 Infusion Pumps in a biomedical technical service environment. It functions to retrieve and send biomedical settings, and alarm/event logs. The infusion pumps themselves are therapeutic devices, but the DataPort PC is a software accessory for managing those pumps, not a therapeutic device itself.

No

The device is an accessory for infusion pumps, used in a technical service environment to transfer data and manage settings. It does not perform any diagnostic function on a biological system.

Yes

The device is explicitly described as "optional computer (PC) software accessory" and its function is data transfer and management for existing infusion pumps. It does not include any hardware components.

Based on the provided information, the Abbott DataPort PC is not an IVD (In Vitro Diagnostic) device.

Here's why:

  • Intended Use/Indications for Use: The software is described as an "optional computer (PC) software accessory for use exclusively with the Abbott Plum A+ and A+3 Infusion Pumps in a biomedical technical service environment." Its purpose is to support data transfer and management of settings for the infusion pumps.
  • Device Description: The description focuses on the software's ability to retrieve and send data and settings to the infusion pumps.
  • Lack of IVD Characteristics: An IVD device is used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. The Abbott DataPort PC does not interact with patient specimens or perform any diagnostic testing. It is a tool for managing and maintaining medical equipment (infusion pumps).

The software's function is related to the operation and maintenance of the infusion pumps themselves, which are medical devices, but the software itself does not perform an in vitro diagnostic function.

N/A

Intended Use / Indications for Use

The Abbott DataPort PC is an optional computer (PC) software accessory for use exclusively with the Abbott Plum A+ and A+3 Infusion Pumps in a biomedical technical service environment.
The indications for use are the indications for use of the parent devices belonging to the Abbott Plum A+ Infusion Pump family, which are the Abbott Plum A+ and Abbott Plum A+3 Infusion Pumps. Infusion pumps in the Abbott Plum A+ Infusion Pump Family are used in parenteral, enteral and epidural therapies and the administration of whole blood products. The Abbott Plum A+ and A+3 Infusion Pumps are designed to deliver infusions over a broad range of infusion rates from multiple container types.
The device is used in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.

Product codes (comma separated list FDA assigned to the subject device)

FRN

Device Description

The Abbott DataPort PC software supports data transfer between a single computer (PC) and up to 15 Abbott Plum A+ Infusion Pumps, or up to 4 Abbott Plum A 13 Infusion Pumps. Abbott DataPort PC allows authorized users to retrieve infuser alarm logs, event history logs, and biomedical settings from interfaced infusers, and to edit and send modified biomedical settings to the interfaced infusers from the PC.

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

biomedical technical service environment.

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.

K024084, K021350, K011442, K982159

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

§ 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).

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Abbott DataPort PCTM

Special 510(k) / January 2004

JAN 2 9 2004

Ko4o///4

Special 510(K) Summary

    1. Name of Submitter:
      Abbott Laboratories Hospital Products Division 200 Abbott Park Road Abbott Park, Illinois 60064-6133

Establishment Registration # 1415939

2. Manufacturer and Establishment Registration Number:

Abbott Laboratories Hospital Products Division 755 Jarvis Drive Morgan Hill, CA 95037

Establishment Registration # 2921482

    1. Proprietary or Trade Name: Abbott DataPort PC TM
  1. Common Name: Infusion Pump

5. Device Classification, Pancode and ProCode: Class II, 80, FRN

    1. Performance Standards: No performance standards have been established under Section 514 of the Food, Drug and Cosmetic Act for intravenous infusion pumps. Infusion pumps are listed in 21 CFR 880.5725.

7. Intended Use:

The Abbott DataPort PC is an optional computer (PC) software accessory for use exclusively with the Abbott Plum A+ and A+3 Infusion Pumps in a biomedical technical service environment.

8. Indications for Use:

The indications for use are the indications for use of the parent devices belonging to the Abbott Plum A+ Infusion Pump family, which are the Abbott Plum A+ and Abbott Plum A+3 Infusion Pumps. Infusion pumps in the Abbott Plum A+ Infusion Pump Family are used in parenteral, enteral and epidural therapies and the administration of whole blood products. The Abbott Plum A+ and A+3 Infusion Pumps are designed to deliver infusions over a broad range of infusion rates from multiple container types.

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9. Device Description:

The Abbott DataPort PC software supports data transfer between a single computer (PC) and up to 15 Abbott Plum A+ Infusion Pumps, or up to 4 Abbott Plum A 13 Infusion Pumps. Abbott DataPort PC allows authorized users to retrieve infuser alarm logs, event history logs, and biomedical settings from interfaced infusers, and to edit and send modified biomedical settings to the interfaced infusers from the PC.

10. Statement of Substantial Equivalence:

Infusion pumps in the Abbott Plum A+ Infusion Pump Family using the optional Abbott DataPort PC software for data transfer are substantially equivalent to infusion pumps in the Abbott Plum A+ Infusion Pump Family using software programmed by the facility, or a facility contracted software developer, for data transfer.

The Abbott Plum A+ and Abbott Plum A+3 infusers with optional Abbott DataPort PC software are substantially equivalent to currently marketed Abbott Plum A+ and Abbott Plum A+3 infusers using interface software not supplied by Abbott in that:

Similarities:

    1. Both configurations have the same intended use and indications for use.
  • Both configurations use the same fundamental scientific technology. 2)
    1. Both configurations have the same physical, operational, and performance specifications.
    1. Both configurations allow for data transfer via the infuser data communication ports.
    1. Both configurations use the same communication protocol for data transfer.
  • Both configurations use the same accessory hardware for interfacing a PC to the infusers. 6)
    1. Both configurations allow for data transfer from a standalone PC to up to 15 Abbott Plum A+ Infusion Pumps or up to 4 Abbott Plum A+3 Infusion Pumps.
    1. Both configurations are intended for use in a biomedical technician environment.
    1. Both configurations allow for authorized users to retrieve, save, and print alarm and event history logs from connected infusers.
    1. Both configurations do not allow users to program a new therapy into an infuser.
    1. Both configurations do not allow users to enter infuser keystrokes remotely.
    1. Both configurations do not allow users to monitor infusers that are actively infusing, priming, or being programmed for infusion.
    1. Both configurations do not support Hospital Information System / Network interfaces.

Differences:

  • The retrieval, saving, and printing of BioMed configuration settings is possible through the infuser l ) communication dataport with a PC that has the Abbott DataPort PC software installed. BioMed configuration settings cannot be accessed through the infuser communication dataport with a PC using interface software not supplied by Abbott,
  • The editing, saving, and sending of modified BioMed configuration settings is possible through the 2) infuser communication dataport using a PC that has the accessory software installed. BioMed configuration settings cannot be accessed through the infuser communication dataport with a PC using interface software not supplied by Abbott.

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11. Predicate Device Information:

Information for Abbott Plum A+/A+3 Infusion Pumps previously cleared for commercial distribution and determined to be appropriate for use as predicates is provided below.

510(k) #Product NameClearance Date
K024084Abbott Plum A+ Infusion Pump12/31/02
K021350Abbott Plum A+3 Multichannel Infusion Pump05/14/02
K011442Abbott Plum A+ Infusion Pump06/05/01
K982159Abbott Plum A+ Infusion Pump01/12/99

12. Comparison to Legally Marketed Device(s)

| Factors | Subject Device(s)
Abbott Plum A+/A+3 Infusion Pumps (V11.x)
with Abbott DataPort PC | Predicate Device(s)
Abbott Plum A+/A+3 Infusion Pumps (V11.x) |
|----------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------|
| Intended Use | Intended for use at the direction of or under the
supervision of licensed physicians or certified healthcare
professionals for intravenous infusion therapy. | Same |
| Indications for Use | For use in parenteral, enteral and epidural therapies and
the administration of whole blood and blood products. | Same |
| Operating Principle | Infusion of intravenous medications to a patient's
vascular system using a stepper motor in conjunction
with an in-line cassette to meter IV fluids through
dedicated IV administration sets. | Same |
| Administration Sets and
Fluid Contact Materials | Sterile, dedicated, non-pyrogenic administration sets.
"Plum" sets. | Same |
| Physical Features | Size, Weight, Input Lines, Output Lines, Power Sources,
Battery Type, Power Cord, Materials | Same |
| Environmental Features | Operating Temperature, Relative Humidity, Pressure,
Storage Temperature | Same |
| Performance Features | Delivery Rates, VTBI Range, Dose Units, Delivery
Accuracy, Delivery Modes, Distal Occlusion Pressure
Setting, Default Drug Library | Same |
| BioMed Configuration
Settings | Date and Time, Continue Rate, Deliver Together Mode
(Concurrent or Piggyback), Enable Delay Start, Callback
Default (Yes/No), Default Distal Occlusion Pressure,
Max Rate Cap, Default Units/Drug (as listed in Default
Drug Library), Default Dose and Conc Units for Drug | Same |
| Communication Ports | (1) Serial communication dataport for standalone PC
interface with up to (15) Abbott Plum A+ Infusion
Pumps or up to (4) Abbott Plum A+3 Infusion Pumps. | Same |
| Computer Interface
Software | Abbott supplied (optional). | Facility software per the
Abbott Plum A+/A+3
Programmers Guide. |
| Computer (PC) Interface
Software Features | Retrieve, save and print alarm and event history
logs from connected infusers.
Retrieve, save, and print BioMed Settings from
connected infusers.
Edit, save and send modified BioMed Settings to
connected infusers. | Retrieve, save and print
alarm and event history
logs from connected
infusers. |
| Other Features | BarCode Wand (optional) | Same |

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13. Summary of Substantial Equivalence

The Abbott Plum A+Family of Infusion Pumps with the optional Abbott DataPort PC software as described in this submission are substantially equivalent to the predicate Abbott Plum A+ Family of Infusion Pumps in that all the infuser configurations have:

    1. the same intended use,
    1. the same indication for use,
    1. the same fundamental technology and operating principle,
    1. the same physical, environmental and performance features
    1. the same or similar materials of construction for all infuser components,
    1. the same dataport communication capabilities

14. Statement of Safety and Effectiveness

The Abbott Plum A+ Family of Infusion Pumps (V11.x) with Abbott DataPort PC software, meets the functional claims and intended use as described in the product labeling, and is as safe and effective as, the Abbott Plum A+ Family of Infusion Pumps without the Abbott DataPort PC software.

Prepared and submitted on January 19, 2004 by: Garia Melecal Patricia Melerski Manager Regulatory Affairs Device Registration Abbott Laboratories Hospital Products Division D389, J45-2N 200 Abbott Park Road, IL 60064-6133 Phone: 847/938-3718 Fax: 847/938-7867

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Image /page/4/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized graphic of three wavy lines, which is the symbol of the department.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

JAN 2 9 2004

Abbott Laboratories Ms. Patricia Melerski Manager Regulatory Affairs Device Registration Hospital Product Division Department 0389 Building J45-2N 200 Abbott Park Road Abbott Park, Illinois 60064-6133

Re: K040114

K040114
Trade/Device Name: Abbott Plum A+® Infusion Pump with Abbott DataPort PCTM Regulation Number: 880.5725 Regulation Name: Infusion Pump Regulatory Class: II Product Code: FRN Dated: January 19, 2004 Received: January 20, 2004

Dear Ms. Melerski:

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 mendie oonments, or to devices that have been reclassified in accordance with the provisions of Anchanenene, or to are and Cosmetic Act (Act) that do not require approval of a premarket the rederal F UGA). You may, therefore, market the device, subject to the general approvisions 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 (sec above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting (1 Mr.), it may be bacyers in the Code of Federal Regulations, Title 21, Parts 800 to 898. In your device ear or roublish further announcements concerning your device in the Eederal Register.

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Page 2 -Ms. Melerski

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 premained hotelled 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 (301) 594-4618. Also, please note the regulation entifled, "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,

Curls

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 Statement 510(k) K640114 Number (if known) Device Abbott Plum A+® Infusion Pump with Abbott DataPort PCTM Name: The Abbott Plum A+® Infusion Pump with Abbott DataPort PCTM Indications has the following indications for use: The device is used in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.

PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED

Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use (per 21 CFR 801.109)

OR

Over-The Counter Use _________________________________________________________________________________________________________________________________________________________

Nicole Dillard, Interim Branch Chief

(Division Sign-Off) General Hospital, (Division of Anesthesiology Division Control, Dental D

510(k) Number: K040114