(363 days)
Not Found
No
The summary describes a standard infusion pump with no mention of AI or ML capabilities, image processing, or data sets typically associated with AI/ML development.
Yes
The device is described as an "Infusion Pump" that provides "controlled delivery of fluids, blood and blood products" for various applications including "intravenous applications". Infusion pumps are typically used to administer medication or fluids to patients, which classifies them as therapeutic devices.
No
Explanation: The device is described as an "Infusion Pump" used for "controlled delivery of fluids, blood and blood products". This indicates a therapeutic function (delivering substances to the body) rather than a diagnostic one (identifying a disease or condition).
No
The device description explicitly states "Linear Peristaltic Infusion Pump," which is a hardware device. The intended use also describes the delivery of fluids, blood, and blood products, which requires a physical pump mechanism.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for the "controlled delivery of fluids, blood and blood products" for various applications within the body (enteral, epidural, subcutaneous, arterial, and intravenous). This describes a device used on or in a patient for therapeutic or supportive purposes.
- Device Description: A "Linear Peristaltic Infusion Pump" is a device designed to physically move fluids.
- Lack of IVD Characteristics: IVD devices are used to examine specimens (like blood, urine, or tissue) outside the body to provide information about a person's health. The provided information does not mention any analysis of specimens or diagnostic purposes.
Therefore, this device falls under the category of a medical device used for patient care, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
Provides controlled delivery of fluids, blood and blood products and can be used in enteral, epidural, subcutaneous, arterial and intravenous applications.
Product codes (comma separated list FDA assigned to the subject device)
FRN
Device Description
Not Found
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)
Non-clinical tests included accuracy testing and comparison with Sabratek's stated accuracy claim and recording of data.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
+/-5% Flow Accuracy
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
§ 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
2/04/99
510(k) Submission, Sabratek 4040 Infusion Pump
Sabratek, Niles, IL 60714
The following is a Summary of the Sabratek 4040 Infusion Pump substantial equivalence and safety and efficacy.
| Classification Name: | Infusion Pump |
|---|---|
| Common/Usual Name: | Infusion Pump |
| Proprietary Name: | Sabratek 4040 Infusion Pump |
| Classification: | Class II Medical Device |
| Performance Standards: | No applicable performance standards |
| Have been issued under Section 514 of | |
| The Food, Drug and Cosmetic Act. | |
| Predicate Device: | Sabratek 6060 HOMERUN® Volumetric Infusion Pump |
K941984 and Sabratek 3030 Infusion Pump, K914581.
| ELEMENT OF
| COMPARISON | SABRTATEK 4040 PUMP | SABRATEK 6060 PUMP | SABRATEK 3030 PUMP |
|---|---|---|---|
| 510(k)# | K941984 | ||
| Pump type | Linear Peristaltic | Rotary Peristaltic | Linear Peristaltic |
| Intended use(s) | Intravenous, Intra-arterial, | ||
| subcutaneous & intracavity | |||
| infusions | Intravenous, Intra-arterial, | ||
| subcutaneous & intracavity | |||
| infusions | Linear Peristaltic | ||
| Administration Sets | |||
| -Captive Standard Set | Yes | Yes | No |
| -Captive 1.2 Micron Filter | Yes | Yes | No |
| -Captive .22 Micron Filter | Yes | Yes | No |
| -Standard Sabraset | Yes | No | Yes |
| -Approved Competitive Sets | Yes | No | Yes |
| Free Flow Clamp | |||
| -Anti Free Flow Clamp (Set) | Yes | Yes | No |
| -Free Flow Clamp (Pump) | Yes | No | Yes |
| Specific Drug, biologic use: | |||
| -Blood/Blood Products | Blood/Blood Products | No | No |
| Components | |||
| -Pumping Mechanism | Yes | Yes | Yes |
| -Battery | Yes | Yes | Yes |
| -Pressure Sensor | Yes | Yes | Yes |
| -Ultrasound Air In Line | Yes | Yes | Yes |
| Pumping mechanism | Linear Peristaltic | Rotary Peristaltic | Linear Peristaltic |
| Power Requirements | Switchable | ||
| 90-132/138-264Vac 50/60 | |||
| hz | 12 - 18 Volts DC, 50 ma | ||
| maximum | 110V AC, 10 watts, 50/60 | ||
| hz | |||
| Battery Life | 6-6.5 hrs at 125 ml/hr | 25 hrs at 125 ml/hr | 7-8 hrs at 125 ml/hr |
| Recharge Time | 24 hrs | N/A | 24 hrs |
| Fluid Path Material: | |||
| -Tubing | PVC | PVC | PVC |
| -Spike | ABS | ABS | ABS |
| -Check Valve | N/A | N/A | N/A |
| -Silicone Rubber Tubing | Silicone Rubber | Silicone Rubber | Silicone Rubber |
| -1.2 or .22 Micron Filter | Modified acrylic/supor | Modified acrylic/supor | Modified acrylic/supor |
| -MLL (Male Luer Lock) | ABS | ABS | ABS |
| -Connecting Barbs | Acrylic | Acrylic | Acrylic |
| -Y-Site | Acrylic | Acrylic | Acrylic |
| -Fluid Bag | N/A | EVA | N/A |
| -Solvent bonding Solution | Cyclohexanone | Cyclohexanone | Cyclohexanone |
| Infusion Parameters: | |||
| -Flow Rate Range | 0.1 - 999 ml/hr | 0.1 400 ml/hr | 1- 999 ml/hr |
| -Flow Accuracy, % | +/-5% | +/-6% | +/-5% |
| -KO rate | 0.1 - 10 ml/hr | 0.1- 10 ml/hr | 1 - 9 ml/hr |
| -Infusion volume limit | 0.1 - 999.9 ml | 1.1 - 9999 ml | 1 - 999 ml |
| -Prime/purge mode | No | Yes | No |
| Profiles | |||
| -Continuous | Yes | Yes | Yes |
| -Auto-Ramp | Yes | Yes | Yes |
| -Intermittent | Yes | Yes | Yes |
| -25 Period | Yes | Yes | Yes |
| -PCA | No | Yes | No |
| Alarm Type: | |||
| -Air-In-Line | Audible, LCD | Audible, LCD | Audible, LCD |
| -Cassette Not Installed | N/A | Audible, LCD | N/A |
| -Check Internal 9V Batteries | N/A | Audible, LCD | N/A |
| -Complete XX ml (or mg) | Audible, LCD | Audible, LCD | Audible, LCD |
| -Door Open | Audible, LCD | Audible, LCD | Audible, LCD |
| -Down Occlusion | Audible, LCD | Audible, LCD | Audible, LCD |
| -Empty Bag or Up Occlusion | Audible, LCD | Audible, LCD | Audible, LCD |
| -Empty Battery | Audible, LCD | Audible, LCD | Audible, LCD |
| -Hold | Audible, LCD | Audible, LCD | Audible, LCD |
| -Low Bag | None | Audible, LCD | None |
| -Low Battery | Audible, LCD | Audible, LCD | Audible, LCD |
| -Malfunction | Audible, LCD | Audible, LCD | Audible, LCD |
| -Move Tubing | Audible, LCD | None | Audible, LCD |
| -Nicad Depleted | Audible, LCD | Audible, LCD | Audible, LCD |
| -Rate Exceeds Microset Limits | N/A | Audible, LCD | N/A |
| -Release/Remove PCA Cord | N/A | Audible, LCD | N/A |
| -Reprogram | Audible, LCD | Audible, LCD | Audible, LCD |
| -Stuck Key | Audible, LCD | Audible, LCD | Audible, LCD |
| -High Pressure | Audible, LCD | Audible, LCD | Audible, LCD |
| -Low Pressure | Audible, LCD | Audible, LCD | Audible, LCD |
| External Communication | |||
| Capability | Yes | Yes | Yes |
1
510(k) Submission, Sabratek 4040 Infusion Pump
Sabratek, Niles, IL 60714
:
2
| Indications | Provides controlled delivery of fluids, blood and blood
products and can be used in enteral, epidural, subcutaneous,
arterial and intravenous applications. |
|--------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Contraindications | The Sabratek 4040 Infusion Pump is contraindicated for use
with a blood set, other than those specifically designated as
such and manufactured by Sabratek Corporation. |
| Non-Clinical Tests | Non-clinical tests included accuracy testing and comparison
with Sabratek's stated accuracy claim and recording of data. |
| Conclusions | The Sabratek 4040 Infusion Pump is equivalent in safety and
efficacy to its predicate devices. |
3
Image /page/3/Picture/1 description: The image is a black and white seal for the Department of Health & Human Services - USA. The seal is circular with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract image of an eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
FEB 2 4 1999
Mr. Charles P . Gill Manager, Regulatory Affairs Sabratek Corporation 8111 North St.Louis Avenue Skokie, Illinois 60076
K980751 Re : Sabratek 4040 Infusion Pump Trade Name: Requlatory Class: II Product Code: FRN Dated: November 13, 1998 December 3, 1998 Received:
Dear Mr. Gill
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 You may, therefore, Food, Drug, and Cosmetic Act (Act). market the device, subject to the general controls provisions The general controls provisions of the Act 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 regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. ಕ್ಕೆ substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) requlation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory 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
4
Page 2 - Mr. Gill
the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
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) 594-4692. 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" (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.fdag.gov/cdrh/dsmamain.html".
Sincerely yours,
Timothy A. Ulatowski
Directbr Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
ﻴﺔ
510(k) Number (if Known)
Device Name: Sabratek 4040 Infusion Pump
Provide controlled delivery of fluids, blood and blood products and can be Indications for use: used in enteral, epidural, subcutancous, arterial and intravenous applications.
Prescription Device. Federal Law (US) restricts this device to sale by or on the order of a physician.
(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 -----
Labacia Cucente (Optional Format 1-2-96)
(Division)
(Division Sign-Off) Division of Denial. Infection Control, and General Hospital Devices
510(k) Number K980751