← Product Code [FRN](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FRN) · K040114 # ABBOTT DATA PORT PC, MODEL 12181 (K040114) _Abbott Laboratories · FRN · Jan 29, 2004 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FRN/K040114 ## Device Facts - **Applicant:** Abbott Laboratories - **Product Code:** [FRN](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FRN.md) - **Decision Date:** Jan 29, 2004 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 880.5725 - **Device Class:** Class 2 - **Review Panel:** General Hospital - **Attributes:** Software as a Medical Device ## 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. ## Device Story Abbott DataPort PC is an optional software accessory for Abbott Plum A+ and A+3 Infusion Pumps. Used in biomedical technical service environments by technicians to manage pump configurations. Software interfaces with up to 15 Plum A+ or 4 Plum A+3 pumps via serial communication dataport. Enables retrieval, saving, and printing of alarm logs, event history, and biomedical settings. Allows editing and uploading of modified biomedical settings to pumps. Does not support remote programming of therapies, remote keystrokes, or active monitoring of infusion/priming. Benefits include centralized management of device settings and maintenance logs, improving efficiency for biomedical staff. ## Clinical Evidence No clinical data. Bench testing only. ## Technological Characteristics Software accessory for serial communication with infusion pumps. Uses existing pump data communication ports and protocols. Connectivity: Standalone PC to pump interface. No changes to pump hardware, materials, or infusion delivery mechanisms. ## Regulatory 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. ## Predicate Devices - Abbott Plum A+ Infusion Pump ([K024084](/device/K024084.md)) - Abbott Plum A+3 Multichannel Infusion Pump ([K021350](/device/K021350.md)) - Abbott Plum A+ Infusion Pump ([K011442](/device/K011442.md)) - Abbott Plum A+ Infusion Pump ([K982159](/device/K982159.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}------------------------------------------------ ## 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 - 3. Proprietary or Trade Name: Abbott DataPort PC TM 4. Common Name: Infusion Pump #### 5. Device Classification, Pancode and ProCode: Class II, 80, FRN - 6. 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. {1}------------------------------------------------ #### 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) - 3) Both configurations have the same physical, operational, and performance specifications. - 4) Both configurations allow for data transfer via the infuser data communication ports. - 5) 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) - 7) 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. - 8) Both configurations are intended for use in a biomedical technician environment. - 9) Both configurations allow for authorized users to retrieve, save, and print alarm and event history logs from connected infusers. - 10) Both configurations do not allow users to program a new therapy into an infuser. - 11) Both configurations do not allow users to enter infuser keystrokes remotely. - 12) Both configurations do not allow users to monitor infusers that are actively infusing, priming, or being programmed for infusion. - 13) 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. {2}------------------------------------------------ ## 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 Name | Clearance Date | |----------|--------------------------------------------|----------------| | K024084 | Abbott Plum A+ Infusion Pump | 12/31/02 | | K021350 | Abbott Plum A+3 Multichannel Infusion Pump | 05/14/02 | | K011442 | Abbott Plum A+ Infusion Pump | 06/05/01 | | K982159 | Abbott Plum A+ Infusion Pump | 01/12/99 | ## 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 | {3}------------------------------------------------ .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ### 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, - 2) the same indication for use, - 3) the same fundamental technology and operating principle, - 4) the same physical, environmental and performance features - 5) the same or similar materials of construction for all infuser components, - 6) 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 {4}------------------------------------------------ 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. {5}------------------------------------------------ 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 {6}------------------------------------------------ # 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 --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FRN/K040114](https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FRN/K040114) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com