Guidewires
Nitinol Guidewire
by Argon Medical Devices, Inc.
A long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Nitinol Guidewire 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 |
|---|---|---|---|
| 190118040 | — | Not stated | Available |
| 190118080 | — | Not stated | Available |
FDA clearances
- 510(k) K880288 September 1988
Procedures that use guidewires
Frequently asked questions
What is Nitinol Guidewire used for?
A long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Who makes Nitinol Guidewire?
Nitinol Guidewire is made by Argon Medical Devices, Inc.. It is listed under guidewires in our device library.
What sizes does Nitinol Guidewire come in?
The FDA device database does not list sizes for Nitinol Guidewire. Check the instructions for use or ask a Argon Medical Devices, Inc. representative.
Is Nitinol Guidewire MRI safe?
The FDA device database entry for Nitinol Guidewire does not state its MRI safety status. Check the labeling before MRI.
Is Nitinol Guidewire FDA cleared?
Nitinol Guidewire is covered by FDA submission K880288.
How do I contact a Argon Medical Devices, Inc. sales representative?
Argon Medical Devices, Inc. has not listed representatives on LA Vascular yet. Visit the Argon Medical Devices, Inc. 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.