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Article: BD Announces FDA 510(k) Clearance of BD Vacutainer(R) Rapid Serum Blood Collection Tube.
- Article from:
- PR Newswire
- Article date:
- October 6, 2009
CopyrightCOPYRIGHT 2009 PR Newswire Association LLC. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan. All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)
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Innovative Design Helps Improve Patient Care and Hospital Productivity
FRANKLIN LAKES, N.J., Oct. 6 /PRNewswire/ -- BD Diagnostics - Preanalytical Systems, a unit of BD (Becton, Dickinson and Company), announced today it received U.S. Food and Drug Administration (FDA) 510(k) clearance for the BD VacutainerA' Rapid Serum Tube, a blood collection device designed to help acute healthcare facilities rapidly analyze blood serum for patient diagnosis.
"Blood test results drive many important medical decisions, including how to treat or medicate patients," said Ana Stankovic, MD, Vice President, Medical and Scientific Affairs and Clinical Operations for BD ...