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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: KXA
Date Received: 10/01/2009
Decision Date: 02/12/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: ENDOSCOPE REPROCESSOR OER-PRO
Manufacturer: LAURA STORMS-TYLER
Device Classification Name: Accessories, Cleaning, For Endoscope
Regulation Number: FEB
Classification Product Code: KXA
Date Received: 10/01/2009
Decision Date: 02/12/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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