K Number
K032376
Date Cleared
2003-08-26

(25 days)

Product Code
Regulation Number
870.1200
Panel
CV
Reference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

The ANGIODYNAMICS Accu-Vu Sizing Catheter is for use where angiographic diagnosis is indicated.

Device Description

Not Found

AI/ML Overview

The provided text is a 510(k) premarket notification letter from the FDA to AngioDynamics, Inc. It confirms that the AngioDynamics Accu-Vu Sizing Angiographic Catheter is substantially equivalent to legally marketed predicate devices.

*However, this document does not contain any information regarding acceptance criteria, device performance studies, sample sizes, expert qualifications, ground truth establishment, or any other details typically found in a study report proving a device meets acceptance criteria.

The 510(k) letter is a regulatory approval document based on a submitted application, not the study report itself. To answer your request, I would need access to the actual 510(k) submission (Design History File Number 506), specifically the sections detailing the studies performed to demonstrate substantial equivalence.

Therefore, I cannot fill in the table or provide the requested information based solely on the text you provided.

§ 870.1200 Diagnostic intravascular catheter.

(a)
Identification. An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.(b)
Classification. Class II (performance standards).