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# Teleflex Pacing Guidewire Cleared
- URL: https://www.fdaweb.com/teleflex-pacing-guidewire-cleared/
- Published: 2023-06-07T12:00:00.000Z
- Updated: 2026-09-14T18:37:19.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154630

FDA has cleared a Teleflex 510(k) for its Wattson Temporary Pacing Guidewire – a bipolar temporary device designed specifically for use during transcatheter aortic valve replacement and bicuspid aortic valve procedures. It offers dual functionality, supporting both valve delivery and ventricular bipolar pacing during procedures, the company says. “From its flexible distal pigtail shape to its multiple electrode, bipolar design, the Wattson Temporary Pacing Guidewire is engineered to help reduce the risk of ventricular perforation while providing confidence in capture during rapid pacing,” it says.