New Delhi: Cognota Healthcare on Monday announced that the United States Food and Drug Administration (US FDA) has approved the company’s blood pressure monitor device- ‘COGNOHEALTH Blood Pressure Monitor’, marking the successful foray of the company into the medical devices segment.
The regulatory approval is a significant milestone for Cognota which can now export its blood pressure monitor devices to the US, Europe, and other overseas countries along with tapping the burgeoning Indian market.
Sanjeev Dahiwadkar, Founder & CEO of Cognota Healthcare said, “Hypertension is a critical health problem across the world given the current lifestyle and expectations of people. This silent killer disease is also a huge problem in India after diabetes. Therefore, the US FDA approval of ‘COGNOHEALTH Blood Pressure Monitor’ device is a huge leap in Cognota’s efforts towards addressing this challenge. Built in-house by our R&D team, this approval also vindicates Cognota’s expertise in the successful integration of digital applications with advanced hardware components.