Ablation systems
swiftPro System
A mains electricity (AC-powered) device assembly designed for controlled heating (i.e., temperatures above 43° Celsius) of the body using microwaves, for the treatment of malignant or benign tumours or other disease conditions [e.g., benign prostatic hyperplasia (BPH), prostatitis]. It includes a microwave generator, controls, software (e.g., treatment planning software) and a microwave applicator. It is intended for both whole-body and localized heating of tissues/organs through either externally-mounted components or from catheter- or probe-type applicators inserted topically, endoscopically, or surgically.
swiftPro System 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 |
|---|---|---|---|
| SWF-MIC01 | — | Not stated | Available |
| SWF-SPS01 | — | Not stated | Available |
FDA clearances
- 510(k) K250718 August 2025
- 510(k) K240518 April 2024
Procedures that use ablation systems
Frequently asked questions
What is swiftPro System used for?
A mains electricity (AC-powered) device assembly designed for controlled heating (i.e., temperatures above 43° Celsius) of the body using microwaves, for the treatment of malignant or benign tumours or other disease conditions [e.g., benign prostatic hyperplasia (BPH), prostatitis]. It includes a microwave generator, controls, software (e.g., treatment planning software) and a microwave applicator. It is intended for both whole-body and localized heating of tissues/organs through either externally-mounted components or from catheter- or probe-type applicators inserted topically, endoscopically, or surgically.
Who makes swiftPro System?
swiftPro System is made by Emblation Limited. It is listed under tumor ablation systems (microwave, rf, cryo) in our device library.
What sizes does swiftPro System come in?
The FDA device database does not list sizes for swiftPro System. Check the instructions for use or ask a Emblation Limited representative.
Is swiftPro System MRI safe?
The FDA device database entry for swiftPro System does not state its MRI safety status. Check the labeling before MRI.
Is swiftPro System FDA cleared?
swiftPro System is covered by FDA submissions K240518, K250718.
How do I contact a Emblation Limited sales representative?
Emblation Limited has not listed representatives on LA Vascular yet. Visit the Emblation Limited 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.