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# Teleflex 510(k) Cleared for Arrow VPS Rhythm Device
- URL: https://www.fdaweb.com/teleflex-510-k-cleared-for-arrow-vps-rhythm-device/
- Published: 2017-01-10T12:00:00.000Z
- Updated: 2026-09-14T21:58:52.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137689

FDA has cleared a Teleflex 510(k) for its Arrow VPS Rhythm Device with Optional TipTracker Technology that is intended to provide electrocardiogram-based tip confirmation. The device helps in placement and confirmation of a catheter tip in the superior vena-cava-cavoatrial junction, and it may be used with a range of catheter types and brands. “When paired with the single-use TipTracker Stylet for insertion of peripherally-inserted central catheters, the Arrow VPS Rhythm Device provides real-time visual navigation by tracing the catheter pathway with a blue line on a color screen,” the company says.