Angiographic catheters
Precise Pro
A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Precise Pro models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| PC0730XCE | — | MR Conditional | Available |
FDA clearances
- 510(k) K914007 October 1991
Procedures that use angiographic catheters
Frequently asked questions
What is Precise Pro used for?
A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Who makes Precise Pro?
Precise Pro is made by Cordis US Corp.. It is listed under angiographic catheters in our device library.
What sizes does Precise Pro come in?
The FDA device database does not list sizes for Precise Pro. Check the instructions for use or ask a Cordis US Corp. representative.
Is Precise Pro MRI safe?
The FDA device database lists Precise Pro as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Precise Pro FDA cleared?
Precise Pro is covered by FDA submission K914007.
How do I contact a Cordis US Corp. sales representative?
Cordis US Corp. has not listed representatives on LA Vascular yet. Visit the Cordis US Corp. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.