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FDA 510(k), K072410, KSEA CLEARVISION II, MODEL 40334120
FDA 510(k), K072410, KSEA CLEARVISION II, MODEL 40334120
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510(K) Number: K072410
Device Name: KSEA CLEARVISION II, MODEL 40334120
Manufacturer: KARL STORZ ENDOSCOPY-AMERICA, INC.
Device Classification Name: endoscope, neurological
Regulation Number: 882.1480
Classification Product Code: GWG
Date Received: 08/27/2007
Decision Date: 05/09/2008
Regulation Medical Specialty: Neurology
Device Name: KSEA CLEARVISION II, MODEL 40334120
Manufacturer: KARL STORZ ENDOSCOPY-AMERICA, INC.
Device Classification Name: endoscope, neurological
Regulation Number: 882.1480
Classification Product Code: GWG
Date Received: 08/27/2007
Decision Date: 05/09/2008
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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