Envisionit Deep AI®’s Chest x-ray AI medical device, RADIFY® Triage and notification software, achieves 510(k) FDA clearance.

RADIFY® showed significant clinical accuracy in triaging both pathologies, within an average of 3 seconds to alert healthcare professionals. RADIFY®’s combined speed and accuracy positions it as an essential medical device to enhance the efficiency and effectiveness of medical professionals in emergency rooms and intensive care units. Envisionit Deep AI® was established with a commitment to ethical AI principles. In alignment with this philosophy and to mitigate potential biases in AI, RADIFY® underwent a thorough evaluation using diverse data and pertinent subgroup analysis through RATify, a standalone AI Validation and Quality Assurance tool in the company’s product suite. All the safety parameters of the device were verified in accordance with the software specifications and applicable performance standards and met the acceptance criteria (Device shows 95% AUC).

“In collaboration with Hardian Health, Envisionit Deep AI® diligently showcased the device’s capacity to fulfil precise regulatory benchmarks. The rigorous FDA clearance process involved thorough clinical testing and evaluations, affirming the device’s adherence to the utmost standards of accuracy and safety. Moreover, RADIFY® was one of the first companies that underwent a meticulous evaluation against the FDA’s new robust cybersecurity, rendering the approval even more gratifying.” Hugh Harvey, Managing Director Hardian Health.

“RADIFY®’s ability to quickly triage pneumothorax and pleural effusion significantly reduces the time taken to alert ER doctors to critical pathologies that require urgent attention. This innovative solution is a game changer that will enhance the efficiency of doctors leading to better patient care”, said Dr. Steven Holt, CEO, First Care Solutions.