FDA 510(k), K093106, ENDOSCOPE REPROCESSOR OER-PRO

FDA 510(k), K093106, ENDOSCOPE REPROCESSOR OER-PRO

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510(K) Number: K093106
Device Name: ENDOSCOPE REPROCESSOR OER-PRO
Manufacturer: LAURA STORMS-TYLER
Device Classification Name: Accessories, Cleaning, For Endoscope
Regulation Number: FEB
Classification Product Code: 10/01/2009
Date Received: 02/12/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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