SILCLEAR TUBING (MODIFICATION)

K953864 · Degania Silicone , Ltd. · FPK · Nov 6, 1995 · General Hospital

Device Facts

Record IDK953864
Device NameSILCLEAR TUBING (MODIFICATION)
ApplicantDegania Silicone , Ltd.
Product CodeFPK · General Hospital
Decision DateNov 6, 1995
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 880.5440
Device ClassClass 2

Indications for Use

The color coded tubing can be used in a variety of situations in the laboratory or hospital where coding is desirable.

Device Story

Transparent silicone tubing with extruded radiopaque or colored stripes within tubing wall; used in laboratory or hospital environments for fluid transport or identification; color coding facilitates organization; manufactured via extrusion in environmentally controlled areas; biocompatibility verified via USP Class VI testing for masterbatch pastes and barium sulfate; intended for clinical or laboratory staff use.

Clinical Evidence

Bench testing only. Biocompatibility evaluated per ISO 10993-1 and U.S. FDA Tripartite Guidance for up to 30-day tissue contact. Materials (silicone masterbatch pastes and barium sulfate) tested to USP Class VI standards.

Technological Characteristics

Transparent silicone tubing; extruded internal color-coded or radiopaque stripes; materials include silicone masterbatch pastes and barium sulfate; manufactured in environmentally controlled area; biocompatibility compliant with ISO 10993-1 and USP Class VI.

Indications for Use

Indicated for use in laboratory or hospital settings requiring tubing identification via color coding. No specific patient population, age, or disease state contraindications provided.

Regulatory Classification

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.

Special Controls

*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.

Predicate Devices

Submission Summary (Full Text)

{0} NOV - 6 - 3 - Degania Silicone Degania Silicone Ltd. Degania Bct 15130 Israel Tel: +972 6 755712 Fax: +972 6 755947 Ref. 510 K number K 953864 Product: Silclear Tubing with color coded stripe (Modification) Trade name: Degania Silicone Silclear Tubing Common name: Silicone Tubing Product code: FPK (510 (k) product code of K943992) Device Class: J Classification Panel: General & Plastic Surg Establishment registration number: 8030107 ## 510(K) SUMMARY This summary of 510K safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807: 92. ## DEVICE DESCRIPTION AND USE: The Degania Silicone Silclear Tubing with color coded stripes is a transparent silicone tubing with radiopaque or regular colored stripes extruded inside the tubing wall. The color coded tubing can be used in a variety of situations in the laboratory or hospital where coding is desirable. ## MANUFACTURING: The Degania Silicone Color Coded Tubing is manufactured according to Good Manufacturing Practices and tested according to Standard Operating Procedures in an Environmentally Controlled Area. The manufacturing processes are approximately the same for both the regular and the color coded tubing. ## BIOCOMPATABILITY: The Degania Silicone Tubing (510(k) number K 943992) has been evaluated according to the U.S. FDA TRIPARTITE GUIDANCE and ISO 10993-1 in April/May 1995. The test selection was based on tissue contact for up to 30 days. The full laboratory report is held by Degania Silicone Ltd. The colors are Masterbatch Silicone Pastes that are being used in other products that have been tested to USP Class VI. The Barium Sulfate has been used in other products that have been tested to USP Class VI and Tripartite (up to 30 day tissue contact). Bettel Bettel Lubin Product Advisor Degania Silicone Ltd. Nov. 2, 1995 Date 2'd 28160 9 216 21.91 05 70 101
Innolitics
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