← Product Code [FPA](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA) · K960431 # PRESSURE STOPCOCK/MANIFOLD (K960431) _Scientific Device Manufacturer, LLC · FPA · Oct 29, 1996 · General Hospital · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K960431 ## Device Facts - **Applicant:** Scientific Device Manufacturer, LLC - **Product Code:** [FPA](/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA.md) - **Decision Date:** Oct 29, 1996 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 880.5440 - **Device Class:** Class 2 - **Review Panel:** General Hospital ## Indications for Use This device provides additional access ports into a standard angiographic fluid delivery system and can be used in conjunction with syringes and other accessories where angiographic injection is indicated. This product’s medium/high pressure designation does not preclude its use for low pressure modalities. ## Device Story SDM Angiographic Manifold consists of one or more stopcocks connected in-line; some models include high-pressure extension lines. Device provides additional access ports for angiographic fluid delivery systems; used with syringes and accessories. Operated by clinicians in clinical settings. Polycarbonate body; polyethylene handle plugs; lightly siliconized for rotation. Supplied sterile in Tyvek/Poly pouches. Facilitates fluid delivery during angiography; enables multi-port access for contrast or saline injection. ## Clinical Evidence Bench testing only. Biocompatibility testing performed per ISO 10993, Part I for externally communicating, blood path indirect devices. ## Technological Characteristics Materials: Polycarbonate (body), polyethylene (handle plugs), silicone (lubricant). Configuration: In-line stopcock manifold with optional high-pressure extension lines. Sterilization: Sterile. Biocompatibility: ISO 10993-1 compliant. ## Regulatory 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 - Namic stopcock/manifold devices - Medex stopcock/manifold devices - Spectra Medical stopcock/manifold devices ## 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. 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Sdm OCT 29 1996 999 Andersen Drive, Suite 120 San Rafael, California 94901 Phone 415-454-9370 Fax 415-454-9380 # SUMMARY OF SAFETY AND EFFECTIVENESS K960431 SDM Angiographic Manifold with Extension Lines 510(k) Premarket Notification **Trade Name:** SDM Angiographic Manifold **Generic Name:** Stopcock and Manifold **Manufacturer:** Scientific Device Manufacturer, LLC. 999 Andersen Drive, Suite 110 San Rafael, CA 94901 Establishment Registration Number: TBD ## Classification: In preparation of this PreMarket Notification, it was determined that devices of this generic type have been previously classified as Class II devices. No performance standards have yet been established for these products. ## Product Description: The SDM Angiographic Manifold consists of one or more stopcocks, where the multiple stopcock configurations are connected in line to form a manifold, with some models of each also having a high pressure extension line attached. These devices have bodies made of polycarbonate and handle plugs made of polyethylene. The plugs are lightly siliconized for smooth rotation. Each of the devices will be supplied single packaged and sterile. Packaging will consist of a standard Tyvek/Poly pouch. ## Intended Use: This device provides additional access ports into a standard angiographic fluid delivery system and can be used in conjunction with syringes and other accessories where angiographic injection is indicated. This product’s medium/high pressure designation does not preclude its use for low pressure modalities. {1} ## Rationale for Substantial Equivalence: Scientific Device Manufacturer's Stopcock / Manifolds are substantially equivalent to currently marketed medium and high pressure stopcock / manifold devices with regards to intended use, materials, and design. Dimensions, materials, and functionality have been chosen to replicate several of the predicate devices, including those made by Namic, Medex, and Spectra Medical. No significant changes or modifications were made from those devices. SDM therefore posits that its devices are equivalent in safety and effectiveness to those devices. ## Biocompatibility Evaluation: Materials used in Scientific Device Manufacturer's Angiographic Manifolds were chosen to be generically the same as those present in the substantially equivalent devices. Testing performed by SDM for this externally communicating device (blood path indirect) shows this device to be biocompatible per the requirements of ISO Standard 10993, Part I. ## Summary: Based upon the product description, its intended use, and comparative features of predicate devices, the Scientific Device Manufacturer's Angiographic Manifold is substantially equivalent to other medium and high pressure manifolds currently in use. Richard C. Ball Vice President Regulatory Affairs and Quality Assurance --- **Source:** [https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K960431](https://fda.innolitics.com/submissions/HO/subpart-f%E2%80%94general-hospital-and-personal-use-therapeutic-devices/FPA/K960431) **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