← Product Code [EZL](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EZL) · K181814 # AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water (K181814) _Amsino International, Inc. · EZL · Sep 4, 2018 · Gastroenterology, Urology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EZL/K181814 ## Device Facts - **Applicant:** Amsino International, Inc. - **Product Code:** [EZL](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EZL.md) - **Decision Date:** Sep 4, 2018 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 876.5130 - **Device Class:** Class 2 - **Review Panel:** Gastroenterology, Urology ## Indications for Use Pre-filled Syringe for Balloon Inflation with Sterile Water is intended to be used in inflating foley catheter balloon. ## Device Story The AMSure® Pre-filled Syringe is a single-use, sterile, pre-filled syringe containing USP purified water. It is available in 3cc, 5cc, 10cc, and 30cc volumes. The device is used by healthcare professionals in clinical settings to inflate the retention balloon of a foley catheter. The syringe barrel and plunger are constructed from polypropylene, with a latex-free synthetic rubber plunger gasket and tip cover. The device is gamma-irradiated to ensure sterility. By providing a pre-filled, sterile solution, the device simplifies the catheterization procedure, reduces the risk of contamination associated with manual filling, and ensures the correct volume of sterile water is used for balloon inflation, thereby securing the catheter in the patient's bladder. ## Clinical Evidence No clinical data. Substantial equivalence is supported by bench testing, including functional performance, sterility, and biocompatibility testing (ISO 10993-5, ISO 10993-10). Performance testing confirms compliance with ISO 7886-1, ISO 80369-7, and USP 40 standards. ## Technological Characteristics Materials: Polypropylene (barrel/plunger), pharmaceutical grade latex-free synthetic rubber (gasket/tip cover). Contents: USP purified water. Sterilization: Gamma irradiation. Standards: ISO 7886-1, ISO 80369-7, USP 40, ISO 10993-5, ISO 10993-10. Form factor: 3cc, 5cc, 10cc, 30cc syringes. Single-use. ## Regulatory Identification A urological catheter and accessories is a flexible tubular device that is inserted through the urethra and used to pass fluids to or from the urinary tract. This generic type of device includes radiopaque urological catheters, ureteral catheters, urethral catheters, coudé catheters, balloon retention type catheters, straight catheters, upper urinary tract catheters, double lumen female urethrographic catheters, disposable ureteral catheters, male urethrographic catheters, and urological catheter accessories including ureteral catheter stylets, ureteral catheter adapters, ureteral catheter holders, ureteral catheter stylets, ureteral catheterization trays, and the gastro-urological irrigation tray (for urological use). ## Predicate Devices - Primary Care Solution Pre-Filled 10cc and Pre-Filled 30cc Inflation Syringe with Sterile Water ([K030813](/device/K030813.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}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logos of the Department of Health & Human Services and the U.S. Food & Drug Administration (FDA). The Department of Health & Human Services logo is on the left, featuring a stylized human figure. To the right of that is the FDA logo, with the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text. September 4, 2018 Amsino International, Inc. Cathy Hong Senior RA Specialist 708 Corporate Center Drive Pomona, CA 91768 Re: K181814 > Trade/Device Name: AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Regulation Number: 21 CFR§ 876.5130 Regulation Name: Urological Catheter and Accessories Regulatory Class: II Product Code: EZL Dated: July 6, 2018 Received: July 9, 2018 Dear Cathy Hong: 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 mav, 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 avare 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. 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. {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/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.html; 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 http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm. For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). 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 (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, Image /page/1/Picture/6 description: The image shows the name "Glenn B. Bell -S" in a large, bold font. The text is black and is set against a light background. The letters are clearly legible and evenly spaced. for Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K181814 Device Name AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Indications for Use (Describe) Pre-filled Syringe for Balloon Inflation with Sterile Water is intended to be used in inflating foley catheter balloon, 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) ## 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." FORM FDA 3881 (7/17) {3}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the logo for AMSINO. The logo is in blue and white. The word "AMSINO" is written in large, bold letters. There are two horizontal lines under the word "AMSINO". Worldwide AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Traditional 510(k) Premarket Notification # Section 5: 510(k) Summary #### Submitter Information . - Submitter: Amsino International Inc. 708 Corporate Center Drive, Pomona CA 91768, USA Contact Person: Cathy Hong Senior RA Specialist Phone: +86(21)-69117118 Fax: +86(21)-59148142 E-mail: Cathy Hong@amsino.com Date Prepared: July 06, 2018 #### . Device Information Common or Usual Name: Pre-filled Syringe for Balloon Inflation with Sterile Water Trade or Proprietary Name: AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Product Item: CIS1003, CIS1005, CIS1010, CIS3530 Regulation Number: 876.5130 Classification Name: Urological Catheter and Accessories Device Class: Class II Review Panel: Gastroenterology/Urology Product Code: EZL #### . Predicate Device Information Device Name: Primary Care Solution Pre-Filled 10cc and Pre-Filled 30cc Inflation Syringe with Sterile Water 510(k) Number: K030813 #### . Device Description: - The AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water is a 3cc, 5cc, 10cc and 30cc syringe pre-filled with USP purified water and gamma irradiated. The syringe is produced using polypropylene for the device barrel and plunger and Amsino International, Inc. {4}------------------------------------------------ Image /page/4/Picture/0 description: The image contains the word "AMSINO" in large, bold, white letters against a blue background. There are two horizontal white lines underneath the word. The font is a serif typeface, and the overall design is simple and clean. The logo appears to be for a company or organization named Amsino. Worldwide® AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Traditional 510(k) Premarket Notification pharmaceutical grade latex free rubber for both the plunger gasket and syringe tip cover. The shelf life of AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water is 3 years. There is no prior submission for the AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water. #### ● Indications for Use Pre-filled Syringe for Balloon Inflation with Sterile Water is intended to be used in inflating foley catheter balloon. #### . Product Comparison Summary The proposed AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water is equivalent to the Primary Care Solution, Inc.'s Primary Care Solution Pre-Filled 10cc and Pre-Filled 30cc Inflation Syringe with Sterile Water. The proposed device has the same indications for use, same operation principle, and the same general characteristics with the predicate device. The design and materials of the proposed devices are identical to the predicate device (K030813). | N
o. | Device
Characteristic | Predicate Device | Proposed Device | Comparison
Results | |-------------------------------|------------------------------|---------------------------------------------------------------------------------|---------------------------------------------------------------------------------|-----------------------| | 1 | Product Code | EZL | EZL | Same | | 2 | Indications for
Use | A sterile water pre-filled syringe for use in inflating foley catheter balloon. | A sterile water pre-filled syringe for use in inflating foley catheter balloon. | Same | | 3 | Regulation
Number | 876.5130 | 876.5130 | Same | | 4 | Design
Configuration | Image: syringes | Image: syringes | Similar | | 5 | Principle
of
Operation | Normal | Normal | Same | | 6 | Materials of main components | | | | | | Barrel | Polypropylene | Polypropylene | Same | | | Plunger | Polypropylene | Polypropylene | Same | | | Plunger Gasket | Black pharmaceutical grade,
synthetic rubber (Latex free) | Black pharmaceutical grade,
synthetic rubber (Latex free) | Same | | | Tip Cover | Same as gasket | Same as gasket | Same | | | Solution | Purified water, USP | Purified water, USP | Same | | 7 | Technical
Performance | Conform with ISO7886-1,
ISO 80369-7 and USP 31 | Conform with ISO7886-1,
ISO 80369-7 and USP 40. | Similar | | 8 | Biological
evaluation | Conform with ISO 10993-5,
ISO 10993-10 requirements | Conform with ISO 10993-5,
ISO 10993-10 requirements | Same | | 9 | Sterile method | Gamma Irradiation | Gamma Irradiation | Same | | 1
0 Single
Use/Reusable | Single Use | Single Use | Same | | | | | | | | {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows the word "AMSINO" in a stylized font. The letters are white and are set against a blue background. The font appears to be a serif font, and the letters are bolded. Advancing Healtheare Worldwide "AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Traditional 510(k) Premarket Notification {6}------------------------------------------------ Image /page/6/Picture/0 description: The image shows the word "AMSINO" in a stylized font. The letters are white and have a blue background. There is a blue line above and below the word. re Worldwide AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water Traditional 510(k) Premarket Notification The AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water has the same indications for use and function as the predicate device. The syringe used for the predicate device and proposed device is the same made by Amsino Medical (Kunshan) Co., Ltd. The standards used for the performance test of the proposed device are the latest ones, and the test results meet its requirements. #### . Performance Data The AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water meet the acceptance criterion for all functional, sterility, biocompatibility and other performance criteria which verify it to be substantially equivalent to the predicate devices. Results of the testing demonstrate that there are no new issues of safety and efficacy that are raised with the AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water. #### Conclusions . The information provided within this pre-market notification demonstrates that the AMSure® Pre-filled Syringe for Balloon Inflation with Sterile Water is substantially equivalent to the predicate device. # End of Summary --- **Source:** [https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EZL/K181814](https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/EZL/K181814) **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