DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD

Q: Who is the manufacturer of DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD?

Elcam Medical Acal filed the 510(k) submission for DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD (K123084).

Q: What is the FDA product code for DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD?

FMG. It is classified under 21 CFR 880.5440 as a Class 2 device in the General Hospital panel.

Q: What is the regulatory pathway for DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD?

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

Q: What are the predicate devices for DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD?

Elcam Disposable Stopcock and Manifold (K111016); Scientific Device Manufacturer, LLC SDM Angiographic Manifold (K960431).

Q: Who can help prepare an FDA 510(k) submission like DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD?

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.

K123084 · Elcam Medical Acal · FMG · May 23, 2013 · General Hospital

Device Facts

Record ID	K123084
Device Name	DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD
Applicant	Elcam Medical Acal
Product Code	FMG · General Hospital
Decision Date	May 23, 2013
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 880.5440
Device Class	Class 2

Indications for Use

Elcam's High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended to serve as flow control and delivery devices for I.V fluids injection to the patient's vascular system. The devices are indicated for medium and high pressure injection of fluids such as, but not limited to, fluids used during angiography and angioplasty and during interventional radiology and cardiology procedures. Devices indication for medium and high pressure does not preclude its use for low pressure procedures. The High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended for single use only.

Device Story

Stopcocks and manifolds function as flow control and delivery interfaces for I.V. fluids; used in cardiac angiography, angioplasty, interventional radiology, and cardiology. Devices connect to I.V. sets to manage fluid administration; units can be used individually or ganged together as manifolds. Designed to withstand high-pressure injections (up to 1200 psi) compared to standard low-pressure stopcocks. Operated by clinicians in clinical settings. Provides a secure, pressure-resistant pathway for contrast media or other fluids; ensures integrity during high-pressure procedures; prevents leakage or failure under stress. Single-use, disposable design.

Clinical Evidence

Bench testing only. Performance validated via high-pressure testing per ISO 8536-10, biocompatibility per ISO 10993, and sterilization/packaging integrity per ISO 11135-1 and ISO 11607. No clinical data required for this device type.

Technological Characteristics

Materials: Polycarbonate LEXAN (body/rotator), ACETAL-ULTRAFORM (handle), Liquid Silicone Rubber (O-ring). Pressure ratings: 500-1200 psi depending on model. Standards: ISO 8536-10 (pressure), ISO 594-1/2 (connectors), ISO 10993 (biocompatibility), ISO 11135-1 (sterilization), ISO 11607-1/2 (packaging). Sterilization: EtO. Form factor: Stopcock and manifold configurations.

Indications for Use

Indicated for patients undergoing angiography, angioplasty, interventional radiology, or cardiology procedures requiring medium or high-pressure fluid injection into the vascular system. Suitable for use in low-pressure procedures as well. Single-use only.

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

Elcam Disposable Stopcock and Manifold (K111016)
Scientific Device Manufacturer, LLC SDM Angiographic Manifold (K960431)

Submission Summary (Full Text)

{0}------------------------------------------------ # K123084 Image /page/0/Picture/1 description: The image contains a logo for Elcam Medical. The logo consists of a stylized letter "E" on the left, followed by the text "Elcam" in a bold, sans-serif font. Below "Elcam" is the word "MEDICAL" in a smaller, sans-serif font. Underneath the logo is the text "Where everything connects" in a smaller font. Dec. 25, 2012 ## 510(k) Summary This 510(k) summary of safety and effectiveness information is submitted in accordance with the requirements of the Safe Medical Devices Act (SMDA) of 1990. The contents of the 510(k) summary have been provided in conformance with 21 CFR §807.92 ## Submitter Information Elcam Medical A.C.A.L. Kibbuts BarAm, M.P. Merom HaGalil, 13860, Israel Tel: (972) 4 6988120/1/2, Fax: (972) 4 6980777 ## Submission contact person: Aharon Cohen Kibuz Bar Am 30889, Israel TEL: 972-4-6988324 ## Device Classification | Proprietary Device Name: | Elcam High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds. | |----------------------------|-------------------------------------------------------------------------------------------| | Common name: | Stopcocks and Manifolds for I.V. | | Product Code: | FMG | | Classification Name: | Stopcock, I.V. Set | | Classification Regulation: | 21 CFR § 880.5440 | | Regulatory Class: | II | ## Identification of the legally Marketed Predicate Devices Elcam's legally cleared Stopcock and Manifold devices (K11016) are indicated for flow control and delivery of I.V drugs and fluids used in I.V procedures. Devices are intended for normal pressures of gravity feed, sampling and bolus injection. Scientific Device Manufacturer, LLC's cleared SDM Angiographic Manifold devices (K96031) are intended for I.V medium and high pressure fluids injection, used in angiography procedures. Above legally Marketed Devices used as substantial equivalence to Elcam proposed High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds (modified version of the legally cleared Stopcock and Manifold devices - K111016) ## Device Description Stopcocks and Manifolds are generally used for administration of fluids into the human. body. There is a wide use of Stopcocks as flow controls and sampling sites in I.V sets, critical care applications and monitoring kits. Stopcocks are used individually or in the form of Manifolds, units comprised of several Stopcocks joined together ("gang"). {1}------------------------------------------------ High pressure Stopcocks and Manifolds are used in cardiac angiography and angioplasty procedures in which fluids are administered under pressure. These procedures require stopcocks and manifolds which are robust under high pressures. The line of pressure resistant Stopcocks and Manifolds presented in this file includes four (4) products: - i. High Pressure (HP) Stopcocks - ii. Medium Pressure (MP) Stopcocks - High Pressure (HP) Manifolds iii. - Premium High Pressure (PHP) Manifolds iv. ## Intended Use of Device Elcam's High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended to serve as flow control and delivery devices for I.V fluids injection to the patient's vascular system. The devices are indicated for medium and high pressure injection of fluids such as, but not limited to, fluids used during angiography and angioplasty and during interventional radiology and cardiology procedures. Devices indication for medium and high pressure does not preclude its use for low pressure procedures. The High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended for single use only. #### Safety & Effectiveness The proposed and predicate devices are similar in design, materials of construction, components, intended use and labeling. Based on the performance results provided (including test results and clinical data) and the analysis of similarities and differences presented above, Elcam Medical believes that the proposed device safe & effectiveness is substantially equivalent to the predicate device without raising new safety and/or effectiveness issues. ### Rational for Substantial Equivalency Substantial equivalency between the proposed devices, to its predicate devices was demonstrated by comparison in a tabular way of the intended use, indications, effectiveness, safety, performance and basic technological characteristics. | # | Comparison parameter | Proposed device: Elcam Disposable High Pressure Stopcock/Manifold | Elcam Disposable Stopcock/ Manifold | Scientific Device Manufacturer, LLC- SDM Angiographic Manifold | |---|-------------------------|-------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------| | 1 | K No. | K123084 | K111016 | K960431 | | 2 | Owner | Elcam Medical A.C.A.L. | Elcam Medical A.C.A.L. | Scientific Device Manufacturer, LLC | | 3 | components materials | The device is composed of the following materials: Body: Polycarbonate LEXAN Handle: ACETAL- | The product is made of the following materials: Body: Former Lexan Handle: High Density | The product is made of the following materials: - Handle - Acetal | #### SE discussion: {2}------------------------------------------------ | # | Comparison parameter | Proposed device: Elcam Disposable High Pressure Stopcock/Manifold | Elcam Disposable Stopcock/ Manifold | Scientific Device Manufacturer, LLC- SDM Angiographic Manifold | |---|------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | | ULTRAFORM High Pressure Rotator: Polycarbonate LEXAN O-Ring: Liquid Silicone Rubber (Apple Rubber) | Polyethylene | O-Ring- Ethylene Propylene Terpolymer Rubber (EPDM) Body-Polycarbonate Handle plugs - Polyethylene | | 2 | Pressure Rating | HP Stopcocks - 1200 psi (82 Bar) MP Stopcocks - 500 psi )35 Bar) HP Manifold - 600 psi (41.3 bar) PHP Manifolds - 800 psi (54.6 bar) | Pressure is up to 3 bar (44 psi) | Pressure Ranges 500 -1200psi | | 3 | Performance parameters | Designed to withstand high pressure injections | Not designed to withstand high pressure injections | Designed to withstand high pressure injections | | 4 | Integrity of materials and functionality after EtO sterilization | The materials and the product functionality are not affected by EtO sterilization process or as a result of aging over rated life time specification. | The materials and the product functionality are not affected by EtO sterilization process or as a result of aging over rated life time specification. | The materials and the product functionality are not affected by EtO sterilization process or as a result of aging over rated life time specification. | | 5 | Biocompatibil ity standards | Tests performed according to ISO 10993 | Test performed according to ISO 10993 | Test performed according to ISO 10993 | | 6 | Performance Standards | Tests performed according to: ISO 8536-10 ISO 594-1 ISO 594-2 | Tests performed according to: ISO 594-1 ISO 594-2 | Unknown | | 7 | Sterilization and sterile package integrity | Tests performed according to: ISO 11135-1 ISO 11607-1 and ISO 11607-2 | Tests performed according to: ISO 11135-1 ISO 11607-1 and ISO 11607-2 | Unknown | The above table compares similarities and differences between Elcam's High Pressure Stopcock/Manifold to legally cleared Elcam Stopcock and Manifold devices (K111016) and to Scientific Device Manufacturer, LLC-SDM Angiographic Manifold (K960431). The following summarizes the main tests performed to demonstrate substantial equivalence resulting from the use of different materials required for sustaining high pressure injection: - High pressure performance tests for conformity to ISO 8536-10 standard . - Biocompatibility . - Integrity of materials and functionality after EtO sterilization . - Sterilization and sterile package integrity tests for conformity to ISO 11135-1, ISO . - l 1607-1 and ISO 11607-2 #### Conclusion The mentioned nonclinical tests and clinical use experience of Elcam's predicate legally marketed Disposable Stopcock/ Manifold demonstrate that the Disposable High Pressure Stopcock/Manifold is as safe, as effective, and performs as well as or better than the legally marketed devices identified in the K123084 submission. {3}------------------------------------------------ #### Substantial Equivalence Statement Based on the above, it is Elcam Medical's opinion that the proposed Elcam High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are substantially equivalent in terms design principles, performance features and of safety & effectiveness to the legally cleared predicate devices : Elcam's Disposable Stopcocks/ Manifolds (K111016) and to Scientific Device Manufacturer, LLC's- SDM Angiographic Manifold (K960431), referred to in chapter 4 of this 510(K) submission executive summary document. {4}------------------------------------------------ #### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 #### May 23, 2013 Mr. Aharon Cohen Regulatory Affairs Manager Elcam Medical A.C.A.L. Kibbutz Bar-Am D.N. Merom Hagalil Israel 13860 Re: K123084 Trade/Device Name: Elcam High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds Regulation Number: 21 CFR 880.5440 Regulation Name: Intravascular Administration Set Regulatory Class: II Product Code: FMG Dated: April 3, 2013 Received: April 25, 2013 Dear Mr. Cohen: 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. 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. {5}------------------------------------------------ #### Page 2 - Mr. Cohen 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 (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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 the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely yours, Susan Runner, DOSIA Digitally signed by Mary S. Runner -S ON: c=US, o=U.S. Government, ou=HHS, ou=FDA, ou=People, cn=Mary S. Runner 0.9.2342.19200300.100.1.1=1300087950 Date: 2013.05.23 14:13:45 -04'00' Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ ## Indications for Use 510(k) Number (if known): K......................... Device Name: Elcam High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds #### Indications for Use: Elcam's High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended to serve as flow control and delivery devices for I.V fluids injection to the patient's vascular system. The devices are indicated for medium and high pressure injection of fluids such as, but not limited to, fluids used during angiography and angioplasty and during interventional radiology and cardiology procedures. Devices indication for medium and high pressure does not preclude its use for low pressure procedures. The High and Medium Pressure Stopcocks and High and Premium High Pressure Manifolds are intended for single use only. Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) #### Concurrence of CDRH, Office of Device Evaluation (ODE) Image /page/6/Picture/10 description: The image shows the FDA logo. The logo is made up of the letters FDA in a stylized font. The letters are outlined in black and the inside of the letters are white. The logo is simple and recognizable. Richard C. Chapman 2013.05.23 13:56:27 -04'00' (Division Sign-Off) (Division Sign-On) Division of Anesthesiology, General Hospital Division Control, Dental Devices Page 1 of 1 **510(k) Number:** K12084

DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD

Device Facts

Indications for Use

Device Story

Clinical Evidence

Technological Characteristics

Indications for Use

Regulatory Classification

Identification

Special Controls

Predicate Devices

Submission Summary (Full Text)

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DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD

Device Facts

Indications for Use

Device Story

Clinical Evidence

Technological Characteristics

Indications for Use

Regulatory Classification

Identification

Special Controls

Predicate Devices

Submission Summary (Full Text)

Panel 1

Section Matches

Product Code Matches

Special Control Matches

My Alerts

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