Who is the manufacturer of Sterile Syringes for Single Use?

Shanghai Kindly Enterprise Development Group Co., Ltd. filed the 510(k) submission for Sterile Syringes for Single Use (K223678).

What is the FDA product code for Sterile Syringes for Single Use?

FMF. It is classified under 21 CFR 880.5860 as a Class 2 device in the General Hospital panel.

What is the regulatory pathway for Sterile Syringes for Single Use?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like Sterile Syringes for Single Use?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Sterile Syringes for Single Use

Q: What are the predicate devices for Sterile Syringes for Single Use?

DMC Medical Single-use Polycarbonate Syringe (K103736).

K223678 · Shanghai Kindly Enterprise Development Group Co., Ltd. · FMF · Feb 9, 2023 · General Hospital

Device Facts

Record ID	K223678
Device Name	Sterile Syringes for Single Use
Applicant	Shanghai Kindly Enterprise Development Group Co., Ltd.
Product Code	FMF · General Hospital
Decision Date	Feb 9, 2023
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 880.5860
Device Class	Class 2
Attributes	Therapeutic

Intended Use

Sterile Syringes for Single Use are sterile, single-use, disposal, without needle and manually operated syringes intended to use with a 6% conical fitting device for injection of drug into the body. The syringes are intended for use immediately after filling and are not intended to contain the fluid/medication for extended periods of time.

Device Story

Sterile, single-use, manually operated piston syringes; used for drug injection. Components: polycarbonate barrel, plunger, polyisoprene rubber piston, medical-grade silicone lubricant. Universal luer threaded connector (ISO 80369-7). Operated by healthcare professionals in clinical/hospital settings. User connects syringe via luer, manually advances/withdraws plunger to express/withdraw fluids. Fluid volume measured via printed external scale on barrel. Benefits: provides sterile, disposable means for drug delivery. No clinical data; bench testing only.

Clinical Evidence

No clinical data. Bench testing only. Performance validated per ISO 7886-1 (manual syringes) and ISO 80369-7 (connectors). Biocompatibility per ISO 10993-1 (cytotoxicity, sensitization, irritation, systemic toxicity, pyrogenicity, hemolysis). Particulate matter testing per USP <788>. Sterilization validated per ISO 11135 (EtO). Packaging integrity per ASTM F88/F1929; shipping per ISTA 3A; shelf-life per ASTM F1980.

Technological Characteristics

Materials: Polycarbonate barrel, polyisoprene rubber plunger tip, medical-grade silicone oil (DC 360). Dimensions: 1ml-30ml capacities. Connector: Universal luer threaded (ISO 80369-7). Sterilization: Ethylene Oxide (EtO). Standards: ISO 7886-1, ISO 10993-1, USP <788>, ASTM F88, ASTM F1929, ISTA 3A, ASTM F1980.

Indications for Use

Indicated for injection of drugs into the body using a 6% conical fitting device. Intended for use by healthcare professionals in clinical, hospital, or other healthcare settings. Not for extended storage of medication.

Regulatory Classification

Identification

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

Predicate Devices

DMC Medical Single-use Polycarbonate Syringe (K103736)

Related Devices

K103736 — DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE · Dmc Medical, Ltd. · Jun 10, 2011
K231729 — Sterile syringes for single use with/without needle · Wepon Medical Technology Co., Ltd. · Sep 8, 2023
K191642 — TK Sterile Piston Syringe without Needle · Anhui Tiankang Medical Technology Co., Ltd. · Jan 6, 2020
K213811 — Sterile Hypodermic Syringes for Single Use · Berpu Medical Technology Co., Ltd. · May 12, 2022
K231727 — Sterile Auto-Disable Syringes with/without Needle for Single Use · Wepon Medical Technology Co., Ltd. · Sep 8, 2023

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. February 9, 2023 Shanghai Kindly Enterprise Development Group Co., Ltd. Amv Li Technology Director No. 658 Gaochao Road Shanghai, Shanghai 201803 China Re: K223678 Trade/Device Name: Sterile Syringes for Single Use Regulation Number: 21 CFR 880.5860 Regulation Name: Piston Syringe Regulatory Class: Class II Product Code: FMF Dated: November 05, 2022 Received: December 8, 2022 Dear Amy Li: 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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. {1}------------------------------------------------ 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 of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely. | Courtney | Digitally signed by Courtney Evans -S | | |----------|------------------------------------------|--| | Evans -S | Date: 2023.02.09 11:34:59-05'00' | | For CAPT Alan Stevens Assistant Director DHT3C: Division of Drug Delivery and General Hospital Devices, and Human Factors OHT3: Office of GastroRenal, ObGyn, General Hospital and Urology Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K223678 Device Name Sterile Syringes for Single Use #### Indications for Use (Describe) Sterile Syringes for Single Use are sterile, single-use, disposal, without needle and manually operated syringes intended to use with a 6% conical fitting device for injection of drug into the body. The syringes are intended for use immediately after filling and are not intended to contain the fluid/medication for extended periods of time. Type of Use (Select one or both, as applicable) | <input checked="true" type="checkbox"/> Prescription Use (Part 21 CFR 801 Subpart D) | |-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | <input type="checkbox"/> Over-The-Counter Use (21 CFR 801 Subpart C) | ### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. ### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ # K223678- 510(K) Summary - 1. Date of preparation: February 9, 2023 - 2. Sponsor Identification Shanghai Kindly Enterprise Development Group Co., Ltd. 658 Gaochao Road, Shanghai, 201803, China Contact Person: Hualong Liu Position: Technology Director Tel: +86 02169118232 Email: henry_liu@kdIchina.net - 3. Designated submission correspondent Ms.Amy Lee(Primary Contact Person) Mind-Link Consulting Co., Ltd. Tel: +86 15721449974 Email: amy.li@mind-link.net - 4. Identification of Proposed Device Trade Name: Sterile Syringes for Single use Regulation Number: 21 CFR 880.5860 Regulation Name: Piston syringe Regulatory Class: Class II Product Code: FMF Regulation Number: 21 CFR 880.5860 Review Panel: General hospital - 5. Indication for use Sterile Syringes for Single Use are sterile, single-use, disposal, without needle and manually operated syringes intended to use with a 6% conical fitting device for injection of drug into the body. The syringes are intended for use immediately after filling and are not intended to contain the fluid/medication for extended periods of time. - 6. Device description {4}------------------------------------------------ KDL Sterile Syringes for Single Use are composed of barrel, plunger, and a moveable piston. The plunger does not contact any part of the fluid path, rather the plunger which attaches to the piston and the barrel are fluid path components. Materials of construction for the components have been shown to meet the applicable requirements of ISO 10993-1. Additionally, there is a small amount of lubricant for moving the plunger smoothly along the inside surface of the barrel. The connector is a universal luer threaded style connector. The device is used in general medicine in clinical, hospital, or other settings of healthcare professionals. The Sterile Syringes for Single Use have different specifications, include1ml, 3ml, 10ml, 20ml and 30ml. - 7. Identification of predicate device 510(k) Number: K103736 Product name: DMC Medical Single-use Polycarbonate Syringe # 7.1 Technological Comparison Table with the predicate | Items | Proposed device | Predicate device | Comment | |------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------| | Indications for Use | Sterile Syringes for Single Use are sterile, single-use, disposal, without needle and manually operated syringes intended to use with a 6% conical fitting device for injection of drug into the body. The syringes are intended for use immediately after filling and are not intended to contain the fluid/medication for extended periods of time. | DMC Medical piston type syringes are single use syringes, intended for injecting fluids into or withdrawing fluids from the body. K103736 | Similar Please see Comment 1 | | Description of Submitted Device | Sterile syringes for single use are composed of barrel, plunger, and a moveable piston. The plunger does | DMC Medical Sing-Use Polycarbonate Syringe is offered in the same configurations as the | Same | | | | | | | | not contact any part of the fluid path, rather the plunger which attaches to the piston and the barrel are fluid path components. Individual components are made from properly tested materials included in this submission. Additionally, there is a small amount of lubricant for moving the plunger smoothly along the inside surface of barrel. The connector is a universal luer threaded style connector. The device is used in general medicine in clinical, hospital, or other settings of healthcare professionals. | predicate. It is made from a calibrated hollow barrel, and a moveable piston with a plunger tip at the end of the piston. The piston shaft does not contact any part of the fluid path, rather the tip which attaches to the shaft and the barrel are fluid path components. Individual components are made from properly tested materials included in this submission. Additionally, there is a small amount of lubricant for moving the piston shaft smoothly along the inside surface of barrel. The connector is a universal luer threaded style connector. The device is used in general medicine in clinical, hospital, or other settings of healthcare professionals. | | | | | | 510(k) | | Component and Materials: | | | Same | | Syringe Barrel | Polycarbonate | Polycarbonate | | | Plunger tip | Polyisoprene rubber | Polyisoprene | | | Silicone Oil | Medical Grade Oil(DC 360) | Medical Grade Oil | | | Calibrated Barrel Volume | YES | YES | | | Sterilization method | EtO | EtO | | | 510(k) Approval | This submission | K103736 | | | Principle of Operation | Sterile Syringes for Single Use, the user connects the syringe via the threaded luer, then manually advancing or withdrawing the plunger internal to the barrel, is able to express or withdraw fluids. Fluids are measured via the printed external scale of the barrel; measurements are indicated in ml(milliliters) | The user connects the syringe via the threaded luer, then manually advancing or withdrawing the plunger internal to the barrel, is able to express or withdraw fluids. Fluids are measured via the printed external housing of the barrel; measurements are indicated in ml(milliliters). operation is similar for most | Same | | | | all piston syringes whether fitted with a threaded luer or a slip-fit only end. | | | | | | | | | | | | | Safety and Performances | Conforms to ISO 7886-1:2017. SAL:10-6 Complies with: ISO 10993-1: Evaluation and Testing; Part 4: Selection of tests for interactions with blood; Part 5: Tests for in vitro cytotoxicity; Part 7: Ethylene oxide sterilization residuals; Part 10: Tests for irritation and delayed type hypersensitivity; Part 11: Tests for systemic toxicity, tests for Bacterial endotoxins, Tests for Pyrogenicity And Conforms to USP <788>: Particulate Matter for injection No re-use | DMC Medical syringes conform to the requirements of ISO 7886-1, an FDA recognized standard. Additionally, the Sterility Assurance Level, (SAL) has been established to meet the 10-6 level. The single use syringes are packaged in a way as to ensure conformity with ISO 10993-1, including minimizing residual gases as well as discourage re-use. | Similar Please see comment 2. | | Length (mm) | 1ml: 86.6±0.5 3ml: 80.85±0.5 5ml: 83.5±0.5 10ml: 88.45±0.5 20ml: 96.4±0.5 30ml: 106.8±0.5 | Not Clear. | Difference Please see comment 3. | | Diameter(mm) | 1ml: OD:9.45±0.1 ID: 4.7±0.1 3ml: OD:11.7±0.1 ID: 9.13±0.1 5ml: OD: 15.5±0.1 ID:12.83±0.1 10ml: OD: 19.45±0.1 | Not Clear. | Difference Please see comment 4. | | | | | | | | ID: 16.45±0.1 | | | | | 20ml: | | | | | OD: 22.9±0.1 | | | | | ID: 19.9±0.1 | | | | | 30ml: | | | | | OD: 26.2±0.1 | | | | | ID: 23.7±0.1 | | | | Size of Syringes(ml) | 1, 3, 5, 10, 20, 30 | Not Clear. | Difference Please see comment 5. | | Luer Lock | ISO 80369-7 | ISO 594-2 | Difference Please see comment 6. | | Prescription (Rx) or over the counter | Prescription | Prescription | Same | ### Table 3-1 Technological Comparison Table {5}------------------------------------------------ 510(K) {6}------------------------------------------------ {7}------------------------------------------------ ### SE Comment 1: Indications for Use The proposed device and the predicate device have same indication, that is, they are both intended for injecting fluid into body. But, the predicate device(K103736) has an additional indication, intended for withdrawing fluid from body The proposed device doesn't have this indication. However, the operation principle is same to achieve the indication. Therefore, the difference will not raise new questions on safety and effectiveness of the proposed device and substantially equivalence to the predicate. #### SE Comment 2: Safety and Perform The proposed device and the predicate device have the same test standard for ISO 7886-1 and ISO 10993-serious. But, the proposed device has different models and has added <USP 788> testing. However, all models are tested in accordance with ISO 7886-1 and USP <788> is required for the injection particles to ensure the safe clinical application. Therefore, this difference is considered not to affect the Substantially Equivalency (SE) between the proposed and predicate devices. #### SE Comment 3: Length The proposed device and the predicate device have similar components (Barrel, Plunger, Plunger Stopper) and all comply with ISO 7886-1. However, the differences in dimensions between the proposed device and the predicate are not known. However, dimensional differences do not raise new or different questions of safety and effectiveness. In addition, all barrel lengths and other dimensions have been shown to comply with ISO 7886-1. #### SE Comment 4: Diameter The proposed device and the predicate device have similar components (Barrel, Plunger, Plunger Stopper) and all comply with ISO 7886-1. However, the differences in dimensions between the proposed device and the predicate are not known. However, dimensional differences do not raise new or different questions of safety and effectiveness. In addition, all barrel lengths and other dimensions have been shown to comply with ISO 7886-1. {8}------------------------------------------------ # SE Comment 5: Size of Syringes The proposed device and the predicate device have similar components (Barrel, Plunger, Plunger Stopper) and all comply with ISO 7886-1. However, the differences in dimensions between the proposed device and the predicate are not known. However, dimensional differences do not raise new or different questions of safety and effectiveness. In addition, all barrel lengths and other dimensions have been shown to comply with ISO 7886-1. # SE Comment 6: Luer Lock The proposed device and the predicate device have similar components (Barrel, Plunger, Plunger Stopper) and all comply with ISO 7886-1 However, the differences in test standard for Luer Lock between the proposed device and the predicate are different, the predicated device have finished 510(K) in 2010 and the Luer lock have been tested in accordance with ISO 594-2, but ISO 594-2 was replaced by ISO 80369-7. However, standard number difference does not raise new or different questions of safety and effectiveness. - 8. Non-clinical test conclusion A. Performance testing was validated using the following Standard: - ISO 7886-1:2017 Sterile hypodermic syringes for single use Part 1: Syringes for manual use A - ISO 80369-7:2016 Small-bore connectors for liquids and gases in healthcare applications -A Part 7 : Connectors for intravascular or hypodermic applications. ## B. Biocompatibility The device described in this summary the Sterile Syringe for Single Use were tested and demonstrated to be in conformance to ISO 10993-1 and FDA Guidance "Use of International Standard ISO 10993-1 "Biological evaluation of Medical Devices -Part 1 : Evaluation and Testing within a risk management process". The proposed device is external communicating, blood path indirect, limited <24hr contact duration. - . Cytotoxicity - . Sensitization - Irritation - . Acute Systemic Toxicity - Material-Mediated Pyrogenicity . - Hemolysis ● Particulate Testing using USP <788> Particulate Matter in Injection ### C. Sterilization, Shipping, Shelf-life The proposed device was evaluated for sterility using ISO 11135-Sterilization of healthcare products- Ethylene Oxide -Requirements for the development, validation and routine control of a sterilization process for medical devices - Packaging Integrity Testing ASTM F88/F88M-15 and ASTM F1929-15 - o Seal Strength ASTM F00-09 - Dye Penetration- ASTM F1929 - Simulated Shipping- ISTA 3A:2018 {9}------------------------------------------------ - Shelf-life of 5 years validated using the FDA recognized standard ASTM F1980-16 Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices. - 9. Clinical test conclusion No clinical study is included in this submission. - 10. Conclusion The conclusion drawn from the nonclinical tests demonstrates that the subject device, Sterile Syringes for Single Use are as safe, as effective, and are therefore substantially equivalentto the legally marketed predicate device DMC Medical Single-use Polycarbonate Syringe(K103736).