K Number
K092075
Date Cleared
2009-08-07

(29 days)

Product Code
Regulation Number
870.1250
Panel
CV
Reference & Predicate Devices
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

The St. Jude Medical CPS Direct® SL II Slittable Outer Catheters intended use is designed for intracardiac access of the venous system of the heart and to serve as a conduit during implantation for the delivery of contrast medium and St. Jude Medical devices, including implantable left heart leads and delivery tools, and support of fluids where minimizing blood loss is essential. In addition, the outer guide catheters can work with inner catheters as a system.

Device Description

Not Found

AI/ML Overview

I am sorry, but the provided document discusses a 510(k) premarket notification for a medical device called "CPS Direct® SL II Slittable Outer Catheter." This document is a regulatory letter from the FDA and outlines the substantial equivalence determination for this device.

The information you requested, such as acceptance criteria, details of a study proving device performance, sample sizes, ground truth establishment, and expert qualifications, is not present in this regulatory document. This type of information would typically be found in a detailed study report or a technical capabilities document submitted as part of the 510(k) application, but not in the FDA's decision letter itself.

Therefore, I cannot fulfill your request using only the provided text.

§ 870.1250 Percutaneous catheter.

(a)
Identification. A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.(b)
Classification. Class II (performance standards).