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FDA 510(k), K001408, KSEA VASCULAR FIBERSCOPES
FDA 510(k), K001408, KSEA VASCULAR FIBERSCOPES
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510(K) Number: K001408
Device Name: KSEA VASCULAR FIBERSCOPES
Manufacturer: KARL STORZ ENDOSCOPY-AMERICA, INC.
Device Classification Name: angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 05/04/2000
Decision Date: 10/30/2000
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: KSEA VASCULAR FIBERSCOPES
Manufacturer: KARL STORZ ENDOSCOPY-AMERICA, INC.
Device Classification Name: angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 05/04/2000
Decision Date: 10/30/2000
Regulation Medical Specialty: Gastroenterology/Urology
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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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