DUAL LUMEN CATHETER

K043581 · Acmi Corporation · EYB · Mar 3, 2005 · Gastroenterology, Urology

Device Facts

Record IDK043581
Device NameDUAL LUMEN CATHETER
ApplicantAcmi Corporation
Product CodeEYB · Gastroenterology, Urology
Decision DateMar 3, 2005
DecisionSESE
Submission TypeSpecial
Regulation21 CFR 876.5130
Device ClassClass 2

Intended Use

The dual lumen ureteral catheter is designed for percutaneous and THC uddi lamon aretoral os indicated as a conduit for multiple uses including, but not limited to, ureteral dilation, stone displacement, including, but not limited tial/anesthetic agents and guidewire placement.

Device Story

Dual Lumen Catheter is a ureteral catheter featuring a hollow plastic tube with a flexible tip; designed for insertion into the ureter. Device incorporates two lumens to facilitate simultaneous or sequential passage of guidewires and injection of contrast or anesthetic agents. Operated by clinicians in a clinical setting. Features female luer lock Tuohy-Borst adaptors for connection to external equipment. Soft tip design protects tissue during passage. Modifications from predicate include addition of second lumen, change in material from polyurethane to polyethylene, shortened working length, and color change. Device assists in urological procedures by providing a conduit for therapeutic and diagnostic access.

Clinical Evidence

No clinical data. Substantial equivalence supported by biocompatibility testing and design/performance specifications comparison.

Technological Characteristics

Materials: Polyethylene. Construction: Extruded hollow plastic tube with dual lumens. Features: Flexible tip, female luer lock Tuohy-Borst adaptors. Connectivity: None. Energy source: None (manual).

Indications for Use

Indicated for patients requiring ureteral procedures including ureteral dilation, stone displacement, contrast/anesthetic agent injection, and guidewire placement.

Regulatory Classification

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

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Dual Lumen Catheter ACMI Corporation 136 Turnpike Road Southborough, MA 01772 MAR 3 - 2005 Special 510(k) Notification Summary of Safety and Effectiveness Dec 27, 2004 ### 510(k) Summary of Safety and Effectiveness ACMI Corporation Dual Lumen Catheter K043581 Pg 1 of 3 #### General Information Manufacturer: ACMI Corporation 136 Turnpike Rd. Southborough, MA 01772-2104 Establishment Registration Number: 2020483 Contact Person: Graham A.L. Baillie Senior Regulatory Affairs Specialist Date Prepared: December 27, 2004 Device Description Classification Name: Urological catheter and accessories (21 CFR 876.5130), Class II Trade Name: Dual Lumen Catheter Generic/Common Name: Ureteral Catheter # Predicate Device K930483 Ureteral Catheter (The Flexible Tip (open or closed) Ureteral Catheter) # Intended Uses Dual Lumen Catheter has multiple uses, including ureteral dilation, anesthetic injection, stone displacement, contrast injection, and safe wire/guidewire placement. {1}------------------------------------------------ Southborough, MA 01772 Special 510(k) Notification Summary of Safety and Effectiveness Dec 27, 2004 Kou358i pg 243 #### Product Description Like the predicate Flexible Tip (open or closed) Ureteral Catheter, the Dual Lumen Catheter is a ureteral catheter with a flexible tip used for guidewire placement and for contrast injection. The Dual Lumen Catheter incorporates the same technological characteristics as the predicate device. The proposed Dual Lumen Catheter raises no new questions of safety or effectiveness. Biocompatibility testing confirms that the different materials of construction (from polyurethane to polyethylene) present no new safety concerns. The method of manufacture (extrusion) is the same for both the predicate and the proposed device. The new material used in the Dual Lumen Catheter has been used in other legally marketed devices within the same classification regulation for the same intended use and has had an established history of successful clinical application in Urology. Like the predicate device, the Dual Lumen Catheter features a hollow plastic tube placed inside the ureter, which, as in the predicate device, allows for the passage of guidewires and for the injection of fluid. Both catheters are fitted with female luer lock Tuohy-Borst adaptors, and feature soft tips to ensure protection of tissue during passage. This Special 510(k) proposes an addition of the second lumen to the catheter, a modification of the material characteristics, shortening of the working length and a change of color of the device. The indications for use, principles of operation, and diameter of the Dual Lumen Catheter remain the same as in the predicate device. {2}------------------------------------------------ Dual Lumen Catheter ACMI Corporation 136 Turnpike Road Southborough, MA 01772 Special 510(k) Notification Summary of Safety and Effectiveness Dec 27, 2004 ## Summary of Safety and Effectiveness K 043581 pg 3183 The proposed modifications for the Dual Lumen Catheter, as described in this submission, are substantially equivalent to the predicate device. The proposed modification in design specifications, performance specifications, and dimensional specifications are not substantial changes or modifications, and do not significantly affect the safety or efficacy of the device. {3}------------------------------------------------ Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle symbol on the right. To the left of the eagle, the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion. MAR 3 - 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Graham Baillie Quality Assurance Manager ACMI Corporation 3037 Mt. Pleasant Street RACINE WI 53404 K043581 Re: Trade/Device Name: Dual Lumen Catheter Regulation Number: 21 CFR §876.5130 Regulation Name: Urological catheter and accessories Regulatory Class: II Product Code: 78 EYB Dated. December 27, 2004 Received: December 28, 2004 Dear Mr. Baillie: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your becemined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the encreated of the enactment date of the Medical Device Amendments, or to conniner or prior to may 20, 2011 accordance with the provisions of the Federal Food, Drug, devices mat nave occh receasined require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The r ou may, aterere, mains of the Act include requirements for annual registration, listing of general volided by provisions practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it your device is easonial 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 that a Dederal statutes and regulations administered by other Federal agencies. You must of any I ederal battatos and requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set (21 CFR Part 007), laborning (21 Segulation (21 CFR Part 820); and if applicable, the electronic forth in the quality of over (sions (sections 531-542 of the Act); 21 CFR 1000-1050. {4}------------------------------------------------ This letter will allow you to begin marketing your device as described in your Section 510(k) 10 leval This letter will allow you to begin marketing your antial equivalence of your device to a legally premarket notification. The FDA finding of substantial equivaleered this pe premarket notification. The FDA inding of substantial or 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), please If you desire specific advice for your device of our laceming regulation ( contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter: | 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 | |-----------------|----------------------------------|--------------| | 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 | | 21 CFR 892.xxxx | (Radiology) | 240-276-0120 | | Other | | 240-276-0100 | Also, please note the regulation entitled, "Misbranding by reference to prematic notification" (21 CFR Also, please note the regulation entitled, "Misonalians on your responsibilities under the Act from the (80 807.97). You may obtain other gelleral manon on your copied. Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Nancy C. Brogdon Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ Dual Lumen Catheter ACMI Corporation 136 Turnpike Road Southborough, MA 01772 Special 510(k) Notification Statement of Intended Use Dec 27, 2004 Device Name: Dual Lumen Catheter 510(k) Number: Indications for use: The dual lumen ureteral catheter is designed for percutaneous and THC uddi lamon aretoral os indicated as a conduit for multiple uses including, but not limited to, ureteral dilation, stone displacement, including, but not limited tial/anesthetic agents and guidewire placement. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use: __ X __ Over-the-Counter Use: ________________________________________________________________________________________________________________________________________________________ OR (Per 21 CFR 801.109) David W. Lynn (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number
Innolitics
510(k) Summary
Decision Summary
Classification Order
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