$MFST 510(k) FDA Submission

Medifirst previously announced its 510(k) submission for its Green and Infrared laser devices was accepted by the Center for Devices and Radiological Health (CDRH) of the Food and Drug Administration (FDA) and was assigned a unique document control number. Our consulting company has been in contact with the FDA and we expect to have several updates in the upcoming days and weeks. Continued CEO Schoengood, "This is a very exciting time for Medifirst. The laser devices are very unique and offer an easy-to-use, mobile, affordable and effective product for many different healthcare professionals. The treatment program can serve to enhance their current treatment protocols as well as produce additional revenue streams. While under FDA review, Medifirst will continue to fine-tune and develop its national sales, marketing and social media strategy so it can hit the ground running in anticipation of FDA approval."