(251 days)
Not Found
No
The device description and performance studies focus on the mechanical and fluid dynamics of a needleless IV connector. There is no mention of AI or ML in the intended use, device description, or performance testing.
No.
The device description and intended use indicate it is an accessory for IV administration (a needleless IV connector) designed to eliminate needle-stick injuries and facilitate fluid passage, not to treat a medical condition.
No
Explanation: The Encore™ Neutral is described as a luer activated needleless IV Connector intended for intravenous and blood administrations and aspiration. Its function is to facilitate fluid delivery or withdrawal, not to diagnose a medical condition.
No
The device description clearly outlines a physical, disposable medical device (a luer activated needleless IV Connector) with specific material compositions and mechanical properties, not a software-only product.
Based on the provided text, the Encore™ Neutral is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Intended Use: The intended use clearly states it's for "intravenous and blood administrations and aspiration." This describes a device used on a patient for delivering or withdrawing fluids, not for examining specimens outside the body.
- Device Description: The description focuses on features related to fluid delivery and withdrawal (luer activated, fluid pathway, priming volume, etc.). These are characteristics of devices used in direct patient care.
- Lack of IVD Characteristics: There is no mention of analyzing biological specimens, detecting analytes, or providing diagnostic information based on testing samples in vitro.
Therefore, the Encore™ Neutral is a medical device used for patient care, specifically for intravenous access and fluid management, not an IVD.
N/A
Intended Use / Indications for Use
The Encore™ Neutral is intended for single patient use in intravenous and blood administrations and aspiration without the need for needles, thus eliminating the potential for needle-stick injuries during use.
The Encore™ Neutral may be used with low pressure power injectors having a maximum pressure of 325 psi and a maximum flow rate of 10 mL/sec. The subject device does not have to be changed subsequent to use with a low pressure power injector.
Product codes (comma separated list FDA assigned to the subject device)
FPA
Device Description
The Encore™ Neutral is a luer activated needleless IV Connector that is disposable and for single patient use. It includes the following features:
- smooth swabbable surface
- tight seal integrity with no gaps or openings
- straight-through fluid pathway resulting in zero dead space ●
- 100% effective blood clearing
- neutral fluid displacement ●
- low priming volume
- saline-only flush option
- no clamping sequence or positive pressure syringe technique required
The Encore™ Neutral is a sterile single-use device which is provided individually packaged. The Encore™ Neutral is also provided bulk non-sterile, to be further processed (packaged and sterilized) by another manufacturer.
The Encore™ Neutral is available with an optional protective end cap attached to the male luer of the device.
The Encore™ Neutral is compatible with ISO 594 compliant male luer slip devices and male luer lock devices.
The Encore™ Neutral is composed of medical grade materials that are not made with Bisphenol A (BPA), di-2-ethylhexyl phthalate, diethylhexyl phthalate (DEHP) or natural rubber latex. The materials used have been subjected to and have passed biocompatibility testing per the latest ISO 10993 standards.
The Encore™ Neutral is MR Safe as it does not contain metallic, magnetic or metal components.
The Encore™ Neutral may be used with low pressure power injectors having a maximum pressure of 325 psi and a maximum flow rate of 10 mL/sec. The device does not have to be changed subsequent to use with a low pressure power injector. When used with a low pressure power injector, the Encore™ Neutral must be secured with other devices rated for pressures up to 325 psi with a luer lock connection.
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)
RyMed Technologies, LLC performed design verification performance testing to verify, demonstrate and support the claim of substantial equivalence to the predict device. All testing was conducted on the final finished sterile device.
The following standards were utilized in evaluating the functionality of the Encore ™ Neutral:
- ISO 594-1:1986, Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment -- Part 1: General requirements
- ISO 594-2:1998 Second Edition, Conical Fittings with a 6% (Luer) Taper for Syringes, Needles and Certain Other Medical Equipment- Part 2 Lock Fittings (General Plastic Surgery/General Hospital)
- ASTM F1608-16, Standard Test Method for Microbial Ranking of Porous Packaging Materials (Exposure Chamber Method)
- ASTM F1980-16, Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices
- AAMI/ANSI/ISO 11137-1: 2006/(R)2010, Sterilization of Health Care Products- Radiation- Part 1: . Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices
- AAMI/ANSV/ISO 11137-2:2013. Sterilization of Health Care Products- Radiation- Part 2: Establishing ● the Sterilization Dose
The following performance tests were conducted according to internal procedures. All testing met the predetermined acceptance criteria and support the substantial equivalence determination:
- Activation Force ●
- Flow Rate at Gravity ●
- Fluid Displacement
- Multiple Activations ●
- Back Pressure ●
- Extended Access (Snap Back) ●
- High pressure (static conditions)
- Power Injection 10 mL/sec with maximum pressure of 325 psi ●
- Microbial Ingress
- Mechanical Hemolysis- Injection and Aspiration
- Blood Clearing ●
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.
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
§ 880.5440 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.
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & 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 an abstract symbol that resembles three stylized human profiles facing to the right, stacked on top of each other.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
June 15, 2017
RyMed Technologies, LLC Ms. Anna McCutchen Director of Ouality Assurance and Regulatory Affairs 6000 W. William Cannon Drive B300 Austin, Texas 78749
Re: K162826
Trade/Device Name: Encore™ Neutral Regulation Number: 21 CFR 880.5440 Regulation Name: Intravascular administration set Regulatory Class: Class II Product Code: FPA Dated: May 19, 2017 Received: May 23, 2017
Dear Ms. Anna McCutchen:
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.
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
1
forth in the quality systems (OS) 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 Industry and Consumer Education at its toll-free 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 Industry and Consumer Education 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,
Lori A. Wiggins -S6
Lori A. Wiggins, MPT, CLT Acting Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K162826
Device Name Encore™ Neutral
Indications for Use (Describe)
The Encore™ Neutral is intended for single patient use in intravenous and blood administrations and aspiration without the need for needles, thus eliminating the potential for needle-stick injuries during use.
The Encore™ Neutral may be used with low pressure power injectors having a maximum pressure of 325 psi and a maximum flow rate of 10 mL/sec. The subject device does not have to be changed subsequent to use with a low pressure power injector.
| Type of Use (Select one or both, as applicable) | |
|---|---|
| X Prescription Use (Part 21 CFR 801 Subpart D) | Over-The-Counter Use (21 CFR 801 Subpart C) |
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3
Image /page/3/Picture/0 description: The image shows the logo for RyMed Technologies, LLC. The logo consists of a black square containing a white clover on the left, followed by the text "RyMed" in a bold, sans-serif font. Below "RyMed" is the text "TECHNOLOGIES, LLC" in a smaller, sans-serif font. The logo is simple and professional, with a clear emphasis on the company name.
510(k) Summary
Summary provided per [21 CFR 807.92]- K162826
Date: June 9, 2017
Common Name:
| Submitter's Information: | RyMed Technologies, LLC
6000 W. William Cannon Drive
Building B, Suite 300
Austin, TX 78749
512-301-7334 |
|--------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | |
| Contact: | Anna McCutchen
Director of Quality Assurance and Regulatory Affairs
Phone: (512) 301-7334 x 303
Fax: (512) 301-7338
E-mail: amccutchen@rymedtech.com |
| Device Name/ Trade Name: | Encore™ Neutral |
Needleless IV Connector
Device Classification: Regulation Number: 880.5440, Class II Intravascular Administration Set Classification Product Code: FPA Panel: General Hospital Predicate Device: 510(k) Number: K991653 Device Name: InVision-Plus® Injection Ports Classification Product Code: FPA Regulation Number: 880.5540, Class II Applicant: RyMed Technologies, LLC
Description of the Device
The Encore™ Neutral is a luer activated needleless IV Connector that is disposable and for single patient use. It includes the following features:
- . smooth swabbable surface
- . tight seal integrity with no gaps or openings
- straight-through fluid pathway resulting in zero dead space ●
- 100% effective blood clearing
- neutral fluid displacement ●
- . low priming volume
- saline-only flush option
- . no clamping sequence or positive pressure syringe technique required
4
The Encore™ Neutral is a sterile single-use device which is provided individually packaged. The Encore™ Neutral is also provided bulk non-sterile, to be further processed (packaged and sterilized) by another manufacturer.
The Encore™ Neutral is available with an optional protective end cap attached to the male luer of the device.
The Encore™ Neutral is compatible with ISO 594 compliant male luer slip devices and male luer lock devices.
The Encore™ Neutral is composed of medical grade materials that are not made with Bisphenol A (BPA), di-2-ethylhexyl phthalate, diethylhexyl phthalate (DEHP) or natural rubber latex. The materials used have been subjected to and have passed biocompatibility testing per the latest ISO 10993 standards.
The Encore™ Neutral is MR Safe as it does not contain metallic, magnetic or metal components.
The Encore™ Neutral may be used with low pressure power injectors having a maximum pressure of 325 psi and a maximum flow rate of 10 mL/sec. The device does not have to be changed subsequent to use with a low pressure power injector. When used with a low pressure power injector, the Encore™ Neutral must be secured with other devices rated for pressures up to 325 psi with a luer lock connection.
Indication for Use
The Encore™ Neutral is intended for single patient use in intravenous and blood administrations and aspiration without the need for needles, thus eliminating the potential for needle-stick injuries during use.
The Encore™ Neutral may be used with low pressure power injectors having a maximum pressure of 325 psi and a maximum flow rate of 10 mL/sec. The subject device does not have to be changed subsequent to use with a low pressure power injector.
Substantial Equivalence
The Encore™ Neutral is substantially equivalent to the predicate device having similar indications for use, technological characteristics, and performance. Below is a device comparison between the Encore™ Neutral and the predicate device. In addition, RyMed Technologies, LLC has successfully conducted microbial ingress testing for up to 7 days or 300 activations, and sterilization, shelf life and packaging validations.
5
| Characteristics for Substantial Equivalence (SE) Determination | ||
|---|---|---|
| Characteristic | Predicate Device (K991653) | Encore™ Neutral (subject device) |
| FDA Regulation | 21 CFR 880.5440 | |
| Intravascular Administration Set | ||
| Class II | ||
| Classification Product Code: FPA | 21 CFR 880.5440 | |
| Intravascular Administration Set | ||
| Class II | ||
| Classification Product Code: FPA | ||
| Indications | ||
| for Use | Intended for single patient use in | |
| intravenous and blood administration and | ||
| aspiration without the need for needles, | ||
| thus eliminating the potential for needle- | ||
| stick injuries during use. | Intended for single patient use in | |
| intravenous and blood administration and | ||
| aspiration without the need for needles, | ||
| thus eliminating the potential for needle- | ||
| stick injuries during use. | ||
| Device may be used with low pressure | ||
| power injectors having a maximum | ||
| pressure of 325 psi and a maximum flow | ||
| rate of 10 mL/sec. The subject device does | ||
| not have to be changed subsequent to use | ||
| with a low pressure power injector. | ||
| Design | The predicate device is a luer activated | |
| needleless IV Connector | ||
| The predicate device is disposable and for | ||
| single patient use. | ||
| The predicate device consists of a straight- | ||
| through fluid pathway with zero residual | ||
| volume (dead space), a smooth surface and | ||
| is non-hemolytic (aspiration and injection). | The subject device is a luer activated | |
| needleless IV Connector | ||
| The subject device is disposable and for | ||
| single patient use. | ||
| The subject device consists of a straight- | ||
| through fluid pathway with zero residual | ||
| volume (dead space), a smooth surface and | ||
| is non-hemolytic (aspiration and injection). | ||
| Materials of | ||
| Construction | The predicate consists of the following | |
| medical grade material types: | ||
| Polycarbonate, polyethylene, polyisoprene, | ||
| silicone rubber | The subject device consists of the | |
| following medical grade material types: | ||
| Copolyester, MABS polymer, silicone | ||
| rubber | ||
| Sterilization | The product Sterility Assurance Level | |
| (SAL) is 10-6 | ||
| Method: Gamma and/or Ethylene Oxide | The product Sterility Assurance Level | |
| (SAL) is 10-6 | ||
| Method: Gamma |
6
Comparison
The following differences exist between the subject device and predicate device:
- The subject device indications for use includes use with power injection procedures
- The materials to construct the devices differ
- The subject device is validated for Gamma sterilization while the predicate device may be Gamma or Ethylene Oxide sterilized
The differences in the indications for use for the subject device device do not alter the intended use of the subject device. Both the subject device and predicate device are intended for intravenous and blood administration and aspiration.
The material differences between the subject device and predicate device do not adversely affect the safety and effectiveness of the subject device. All materials are medical grade and have passed biocompatibility testing.
Non-Clinical Data- Performance Testing
RyMed Technologies, LLC performed design verification performance testing to verify, demonstrate and support the claim of substantial equivalence to the predict device. All testing was conducted on the final finished sterile device.
The following standards were utilized in evaluating the functionality of the Encore ™ Neutral:
- . ISO 594-1:1986, Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment -- Part 1: General requirements
- . ISO 594-2:1998 Second Edition, Conical Fittings with a 6% (Luer) Taper for Syringes, Needles and Certain Other Medical Equipment- Part 2 Lock Fittings (General Plastic Surgery/General Hospital)
- ASTM F1608-16, Standard Test Method for Microbial Ranking of Porous Packaging Materials (Exposure Chamber Method)
- ASTM F1980-16, Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices
- AAMI/ANSI/ISO 11137-1: 2006/(R)2010, Sterilization of Health Care Products- Radiation- Part 1: . Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices
- AAMI/ANSV/ISO 11137-2:2013. Sterilization of Health Care Products- Radiation- Part 2: Establishing ● the Sterilization Dose
7
The following performance tests were conducted according to internal procedures. All testing met the predetermined acceptance criteria and support the substantial equivalence determination:
- Activation Force ●
- Flow Rate at Gravity ●
- Fluid Displacement
- Multiple Activations ●
- Back Pressure ●
- Extended Access (Snap Back) ●
- High pressure (static conditions)
- Power Injection 10 mL/sec with maximum pressure of 325 psi ●
- Microbial Ingress
- Mechanical Hemolysis- Injection and Aspiration
- Blood Clearing ●
Biocompatibility
The materials of construction for the subject device were evaluated according to ISO 10993-1:2009 Biological Evaluation of Medical Devices- Part 1: Evaluation and Testing within a Risk Management Process. All testing was conducted on the final finished sterile device. RyMed Technologies, LLC performed testing according to the following parts of the ISO 10993 Standard:
- . ISO 10993-4:2002, Biological Evaluation of Medical Devices- Part 4: Selection of Tests for Interaction with Blood
- ISO 10993-5:2009, Biological Evaluation of Medical Devices- Part 5: Tests for InVitro Cytotoxicity ●
- ISO 10993-10:2010, Biological Evaluation of Medical Devices- Part 10: Tests for Irritation and Skin Sensitization
- ISO 10993-11:2006-, Biological Evaluation of Medical Devices- Part 11: Tests for Systemic Toxicity ●
Conclusion
It is concluded that based on performance data and biocompatibility testing conducted on the subject device along with the same intended use and similarities in indications for use and technological characteristics that the subject device is substantially equivalent to the predicate device.