(11 days)
No
The device description and intended use clearly describe a passive fluid delivery system (extension set) with a needleless access device. There is no mention of any computational or analytical functions that would require AI/ML.
No.
The device is described as an "Extension Set" for administering fluids and aspirating blood through intravascular catheters; it facilitates the delivery of therapy rather than providing therapy itself.
No
The device is an extension set used with intravascular catheters to administer fluids or aspirate blood, not to diagnose conditions.
No
The device description clearly outlines physical components such as tubing, clamps, Luer lock connections, and a split septum device, indicating it is a hardware medical device. There is no mention of software as a component or the primary function.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for aspirating blood or administering fluids, medications, and blood products through intravascular catheters. This is a direct interaction with the patient's circulatory system for therapeutic or diagnostic purposes (like drawing blood for testing elsewhere), not for performing a diagnostic test on a sample in vitro (outside the body).
- Device Description: The description details tubing, connectors, clamps, and a needleless access device. These are components used for fluid management and access to the bloodstream, not for analyzing biological samples.
- No Mention of In Vitro Testing: There is no mention of the device being used to perform tests on biological samples outside of the body.
IVD devices are specifically designed to perform tests on samples like blood, urine, or tissue to diagnose diseases or conditions. This device facilitates the delivery or withdrawal of substances to or from the body, which is a different function.
N/A
Intended Use / Indications for Use
Non-Power Injectable:
Extension Sets with an attached BD Q-Syte™ Luer Access Split Septum are intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood or blood products. These devices may be used with any patient population with consideration given to the procedure being performed and fluids being infused.
Power Injectable:
The Power Injectable Extension Set with an attached BD Q-Syte™ Luer Access Split Septum is intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood or blood products. These devices may be used with any patient population with consideration given to the procedure being performed and fluids being infused.
The Power Injectable Extension Set is also indicated for use with intravascular catheters indicated for power injection of contrast media. The Power Injectable Extension Set is suitable for use with power injectors set to a maximum pressure of 325 psi (2,240 kPa) when the BD Q-Syte device is removed and a direct connection is made.
Product codes
FPA
Device Description
The Extension Sets with BD Q-Syte™ Luer Access Split Septum consist of a length(s) of flexible non-DEHP PVC clear tubing with a non-removable slide clamp. The devices include an ISO male Luer lock connection with a protection cap on the distal end an ISO female Luer lock connection on the proximal end(s) with a removable BD Q-Syte device or end cap. The Extension Sets with BD Q-Syte™ Luer Access Split Septum are provided in lengths from 5 in (127 mm) to 21 in (533 mm) with tubing diameters ranging from 0.035 in ID (0.89 mm) x 0.094 in OD (2.40 mm) to 0.110 in ID (2.80 mm) x .161 in OD (4.10 mm). Select Extension Sets include injection sites with a permanently attached BD Q-Syte device. The BD Q-Syte device is a needleless access device provided to aid in reducing the risk of accidental needlestick injuries. The Extension Sets with BD Q-Syte™ Luer Access Split Septum do not contain natural rubber latex.
The Power Injectable Extension Set with BD Q-Syte™ Luer Access Split Septum is suitable for use with power iniectors set to a maximum of 325 psi (2,240 kPa) when the BD Q-Syte device is removed and a direct connection is made. This device has a label attached to the tubing stating "Power Injectable Max 325 PSI".
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
any patient population
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)
Performance testing was conducted for the predicate devices to demonstrate the integrity and suitability of the device for its intended use. Since the subject devices and currently marketed predicate devices are the same, the results of the predicate testing indicate that the subject Extension Sets with BD Q-Syte™ Luer Access Split Septum are substantially equivalent to the currently marketed predicate devices.
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
§ 880.5440 Intravascular administration set.
(a)
Identification. An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.(b)
Classification. Class II (special controls). The special control for pharmacy compounding systems within this classification is the FDA guidance document entitled “Class II Special Controls Guidance Document: Pharmacy Compounding Systems; Final Guidance for Industry and FDA Reviewers.” Pharmacy compounding systems classified within the intravascular administration set are exempt from the premarket notification procedures in subpart E of this part and subject to the limitations in § 880.9.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
September 19, 2014
Acacia. Incorporated C/O Mr. Mark Job Responsible Third Party Official Regulatory Technology Services, LLC 1394 25th Street, NW Buffalo MN 55313
Re: K142527
Trade/Device Name: Extension Sets with BD O-Syte™ Luer Access Split Septum Regulation Number: 21 CFR 880.5440 Regulation Name: Intravascular Administration Set Regulatory Class: II Product Code: FPA Dated: September 5, 2014 Received: September 8, 2014
Dear Mr. Job:
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 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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.
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Page 2 - Mr. Job
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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
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) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
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Erin I. Keith, M.S. Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
510(k) Number (if known)
Image /page/2/Picture/3 description: The image contains the alphanumeric string "K142527". The text is displayed in a clear, sans-serif font, making it easily readable. The characters are uniformly sized and spaced, contributing to the overall clarity of the image. The background is plain white.
Device Name
Extension Sets with BD Q-Syte™ Luer Access Split Septum
Indications for Use (Describe) Non-Power Injectable:
Extension Sets with an attached BD Q-Syte™ Luer Access Split Septum are intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood products. These devices may be used with any patient population with consideration given to the procedure being performed and fluids being infused.
Power Injectable:
The Power Injectable Extension Set with an attached BD Q-Syte™ Luer Access Split Septurn is intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood or blood products. These devices may be used with any patient population with consideration given to the procedure being performed and fluids being infused.
The Power Injectable Extension Set is also indicated for use with intravascular catheters indication of contrast media. The Power Injectable Extension Set is suitable for use with power injectors set to a maximum pressure of 325 psi (2,240 kPa) when the BD Q-Syte device is removed and a direct connection is made.
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.
SE CONSTITUTION OF THE FOR FOR FOR FOR FOR FOR FOR FOR THE FOR FOR FOR FOR FOR FOR FOR FOR FOR FOR FOR
Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)
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4. 510(k) Summary
This 510(k) summary is being submitted in accordance with 21 CFR 807.92.
| APPLICANT: | Acacia, Inc. |
|---|---|
| ADDRESS: | 785 Challenger Street |
| Brea, CA 92821 | |
| PHONE: | (714) 257-0470 |
| CONTACT PERSON: | Dan Hyun |
| DATE PREPARED: | July 31, 2014 |
| TRADE NAME: | Extension Set with BD Q-Syte™ Luer Access Split Septum |
| COMMON NAME: | Intravascular Extension Set |
| CLASSIFICATION NAME: | Intravascular Administration Set |
| DEVICE CLASSIFICATION: | Class II |
| PRODUCT CODE: | FPA |
| PREDICATE DEVICES: | MPS Acacia Power Injectable Infusion Set (K090809) |
| MPS Acacia IV Extension Sets (K895367) | |
| BD Q-Syte Saf-T PRN Luer Activated Valve (K013621) |
Substantially Equivalent To:
The subject Extension Sets with BD Q-Syte™ Luer Access Split Septum are substantially equivalent in intended use, principal of operation and technological characteristics to the MPS Acacia Power Injectable Infusion Set (K090809), MPS Acacia IV Extension Sets (K895367) and BD Q-Syte™ Luer Access Split Septum (K013621).
All materials, manufacturing methods, technological characteristics, and principles of operation are identical to the predicate devices. The reason for this submission is to clarify and align the Indications for Use for all subject devices. The differences in the indications for use are not considered significant since they do not alter the therapeutic effect of the device, which is to provide a conduit for the infusion and withdrawal of fluids through an intravascular catheter.
Description of the Device Subject to Premarket Notification
The Extension Sets with BD Q-Syte™ Luer Access Split Septum consist of a length(s) of flexible non-DEHP PVC clear tubing with a non-removable slide clamp. The devices include an ISO male Luer lock connection with a protection cap on the distal end an ISO female Luer lock connection on the proximal end(s) with a removable BD Q-Syte device or end cap. The Extension Sets with BD Q-Syte™ Luer Access Split Septum are provided in lengths from 5 in (127 mm) to 21 in (533 mm) with tubing diameters ranging from 0.035 in ID (0.89 mm) x 0.094 in OD (2.40 mm) to 0.110 in ID (2.80 mm) x .161 in OD (4.10 mm). Select Extension Sets include injection sites with a permanently attached BD Q-Syte device. The BD Q-Syte device is a needleless access device provided to aid in reducing the risk of accidental needlestick injuries. The Extension Sets with BD Q-Syte™ Luer Access Split Septum do not contain natural rubber latex.
The Power Injectable Extension Set with BD Q-Syte™ Luer Access Split Septum is suitable for use with power iniectors set to a maximum of 325 psi (2,240 kPa) when the BD Q-Syte device is removed and a direct connection is made. This device has a label attached to the tubing stating
5
"Power Injectable Max 325 PSI".
Indications for Use:
Non-Power Injectable:
Extension Sets with an attached BD Q-Syte™ Luer Access Split Septum are intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood or blood products. These devices may be used with any patient population with consideration given to the procedure being performed and fluids being infused.
Power Injectable:
The Power Injectable Extension Set with an attached BD Q-Syte™ Luer Access Split Septum is intended to be used with intravascular catheters to aspirate blood or administer fluids, including medications and blood or blood products. These devices may be used with any patient population with consideration aiven to the procedure being performed and fluids being infused.
The Power Injectable Extension Set is also indicated for use with intravascular catheters indicated for power injection of contrast media. The Power Injectable Extension Set is suitable for use with power injectors set to a maximum pressure of 325 psi (2,240 kPa) when the BD Q-Syte device is removed and a direct connection is made.
Technical Characteristics:
The subject Extension Sets with BD Q-Syte™ Luer Access Split Septum have the same physical and technical characteristics compared to the currently marketed predicate devices.
Performance Data:
Performance testing was conducted for the predicate devices to demonstrate the integrity and suitability of the device for its intended use. Since the subject devices and currently marketed predicate devices are the same, the results of the predicate testing indicate that the subject Extension Sets with BD Q-Syte™ Luer Access Split Septum are substantially equivalent to the currently marketed predicate devices.
Basis for Determination of Substantial Equivalence:
Upon reviewing the information provided in this submission and comparing intended use, principle of operation and overall technological characteristics, the subject Extension Sets with BD Q-Syte™ Luer Access Split Septum are determined by Acacia to be substantially equivalent to the currently marketed predicate devices.