Neuro aspiration catheters

072 Aspiration System

by Q'apel Medical LLC

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

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072 Aspiration System models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
FG 00806— Not statedAvailable
FG 00995— Not statedAvailable
FG 01252— Not statedAvailable

FDA clearances

  • 510(k) K222786 August 2023

Procedures that use neuro aspiration catheters

Frequently asked questions

What is 072 Aspiration System used for?

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

Who makes 072 Aspiration System?

072 Aspiration System is made by Q'apel Medical LLC. It is listed under neurovascular aspiration catheters, stent retrievers for stroke in our device library.

What sizes does 072 Aspiration System come in?

The FDA device database does not list sizes for 072 Aspiration System. Check the instructions for use or ask a Q'apel Medical LLC representative.

Is 072 Aspiration System MRI safe?

The FDA device database entry for 072 Aspiration System does not state its MRI safety status. Check the labeling before MRI.

Is 072 Aspiration System FDA cleared?

072 Aspiration System is covered by FDA submission K222786.

How do I contact a Q'apel Medical LLC sales representative?

Q'apel Medical LLC has not listed representatives on LA Vascular yet. Visit the Q'apel Medical LLC 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.

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