Healthcare Industry News: US Biologic
News Release - February 25, 2020
EmCyte Announces FDA 510(k) Clearance for its PurePRP(R) Supraphysiologic Concentrating System
FORT MYERS, Fla., Feb. 25, 2020 -- (Healthcare Sales & Marketing Network) -- EmCyte, the world leader in platelet rich plasma and progenitor stem cell biologics, announces its FDA 510(k) clearance for its PurePRP® Supraphysiologic Concentrating System for platelet rich plasma. The system's 510(k) number is BK190317 and is cleared to be used for the safe and rapid preparation of autologous platelet rich plasma (PRP) from a small sample of blood at the patient's point of care. This clearance completes EmCyte's PURE Supraphysiologic product portfolio allowing practitioners to now use the most advanced in autologoUS Biologic concentrating systems."The PurePRP® Supraphysiologic Concentrating System is the next step in clinical excellence," says Patrick Pennie, President & CEO of EmCyte Corporation. "We believe we've hit the mark on this innovation after improving the clinical experience for both the practitioner and patient."
About EmCyte Corporation
EmCyte Corporation®, headquartered in Fort Myers, Florida, is the world leader in platelet rich plasma and progenitor stem cell biologics. Its PURE™ regenerative product solutions have set a new standard in regenerative deliverables with protocol versatility and outstanding recovery performance. EmCyte products are manufactured in its 30,000 square foot manufacturing facility equipped with certified clean rooms and state-of-the-art manufacturing equipment. With over 20 years of experience, EmCyte's commitment to innovation has made a clinical difference in countries around the globe, and its team of qualified experts are available to provide advanced training and clinical support. To learn more about EmCyte Corporation®, visit www.emcyte.com.
Source: EmCyte
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