LMI BILIARY CATHETER

K955126 · Lucas Medical, Inc. · FGE · May 10, 1996 · Gastroenterology, Urology

Device Facts

Record IDK955126
Device NameLMI BILIARY CATHETER
ApplicantLucas Medical, Inc.
Product CodeFGE · Gastroenterology, Urology
Decision DateMay 10, 1996
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 876.5010
Device ClassClass 2
AttributesTherapeutic

Indications for Use

The device is intended for intra-operative short term use in the biliary tree to aid in the removal of ductal stones and debris.

Device Story

Single lumen, stainless steel wire-reinforced silicone catheter; features distal silicone balloon and proximal female luer connector. Used intra-operatively by physicians during biliary surgery. Access via choledochotomy; catheter advanced past stones/debris; balloon inflated to occlude duct; catheter withdrawn to clear stones/debris through access point. Single-use device; EtO sterilized.

Clinical Evidence

Bench testing only; no clinical data provided.

Technological Characteristics

Single lumen silicone tube; stainless steel wire reinforcement; distal silicone balloon; female luer connector; strain relief. EtO sterilized. Single-use.

Indications for Use

Indicated for patients undergoing surgical procedures requiring removal of stones and debris from the biliary tree; for use by or on the order of a physician.

Regulatory Classification

Identification

A biliary catheter and accessories is a tubular flexible device used for temporary or prolonged drainage of the biliary tract, for splinting of the bile duct during healing, or for preventing stricture of the bile duct. This generic type of device may include a bile collecting bag that is attached to the biliary catheter by a connector and fastened to the patient with a strap.

Special Controls

*Classification.* Class II (special controls). The device, when it is a bile collecting bag or a surgical biliary catheter that does not include a balloon component, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.

Predicate Devices

Submission Summary (Full Text)

{0} 03/1996 11:11 714-9380138 LUCAS MEDICAL INC PAGE 03 LMI BILIARY CATHETER LUCAS MEDICAL, INC. 1751 S. DOUGLASS ROAD, ANAHEIM CA 92806 K9551240 510K NOTIFICATION PAGE 1 OF 18 MAY 10 1996 510K SUMMARY PURPOSE: Pursuant to the Federal Food, Drug, and Cosmetic Act, as amended May 28, 1976, Section 510(k), please consider the attached document as Lucas Medical, Inc.'s notification of intent to introduce the LMI Biliary Catheter for commercial distribution. The common names for the device are silicone Biliary catheter and Biliary catheter. BACKGROUND: This 510K submission should be considered as a new application. On March 17, 1995, a 510K was submitted for this product and was issued a reference number of K951310. Additional information was requested on April 4, 1995. In accumulating the data to answer the questions raised, the extension time allotted by the FDA expired. This new 510K submission addresses those earlier questions. MANUFACTURING & STERILIZATION SITES: The manufacturing and packaging facility is: Lucas Medical Inc., 1751 S. Douglass Road, Anaheim CA 92806. The establishment registration number is: 2029386. Sterilization will be performed by Griffith MicroScience (Establishment Registration Number: 2011171) 4900 S. Gilford, Los Angeles CA 90058. DESCRIPTION: The catheter consists of a single lumen stainless steel wire reinforced silicone tube that is end formed to create a rounded leading nose. A silicone balloon is bonded to the distal end of the catheter at the end form. The proximal end of the catheter consists of a female luer connector and a strain relief that are bonded to the silicone shaft. The "DEVICE" is packaged in an EtO breathable tray for protection and then sealed in an EtO breathable pouch. It is EtO sterilized and non-pyrogenic. The "DEVICE" is for Single Use Only and is used only By or On the Order of a Physician. CLASSIFICATION: The "DEVICE" is a Class II Medical device and has a classification number of 78FGE and is reviewed by the Gastroenterology and Urology Review Panel. INTENDED USE: The device is intended for intra-operative short term use in the biliary tree to aid in the removal of ductal stones and debris. PRINCIPLE OF OPERATION: Biliary catheters are generally used in surgical procedures for removal of gall stones in the biliary duct. Access to the bile duct is made through the choledochotomy. The catheter is inserted into the bile duct and advanced beyond the region where stones and debris are present. The balloon is carefully inflated to occlude the bile duct while not overly distending it, and then gently withdrawn to push the stones and debris out of the bile duct at the access point. Once the bile duct has been cleared, the remaining choledochotomy is surgically closed. SUBSTANTIAL EQUIVALENCE: The "DEVICE" is substantially equivalent to the ABI Cathlab Silicone Biliary Catheter which was approved under 510(k) notification K910917. The design parameters and intended use of the "DEVICE" are the same as the substantially equivalent catheter. The "DEVICE" utilizes the same materials of construction and packaging as the substantially equivalent catheter
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