Home » STERIS CORPORATION ANNOUNCES FDA MARKET CLEARANCE OF RELIANCE ENDOSCOPE PROCESSING SYSTEM
STERIS CORPORATION ANNOUNCES FDA MARKET CLEARANCE OF RELIANCE ENDOSCOPE PROCESSING SYSTEM
July 31, 2006
Steris Corporation announced that the United States Food and Drug Administration (FDA) has given the Company clearance to market its Reliance Endoscope Processing System (EPS). The innovative technology of the Reliance EPS addresses significant unmet reprocessing needs within the gastrointestinal (GI) departments of hospitals and surgery centers, including enhanced patient and staff safety, improved quality through an automated, consistent and repeatable process, and increased productivity from faster total reprocessing time.
Steris (http://www.steris.com/CCBN/RELEASEDETAIL.CFM?RELEASEID=887589)
KEYWORDS FDAnews Device Daily Bulletin
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