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# Royal Philips Cardia Transducer for Lumify Cleared
- URL: https://www.fdaweb.com/royal-philips-cardia-transducer-for-lumify-cleared/
- Published: 2016-10-14T12:00:00.000Z
- Updated: 2026-09-14T21:39:41.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137078

FDA has cleared a Royal Philips 510(k) for the S4-1 cardiac transducer for [Lumify](http://www.lumify.philips.com/web/?origin=9%5Fus%5Fen%5Flumify%5Fphilips%5F%5F%5Fcardiac%5Fs41october2016&ref=fdaweb.com), a“smart-device” diagnostic ultrasound solution. The pocket-sized and lightweight device offers high-resolution 2D image quality and exam pre-sets to allow clinicians to quickly triage and assess their patients, the company says. Introduced in 2015, Lumify with the S4-1 transducer expands clinical applications to include a full offering of in-demand cardiac, abdominal, lung, and OB/GYN imaging. Additionally, data will be accessible on the Philips [HealthSuite Digital Platform](http://www.usa.philips.com/healthcare-innovation/research-and-exploration/dreamforce?ref=fdaweb.com), an open and secure, cloud-based infrastructure that allows clinicians and health systems access to data and analytics to help improve patient care, it says.