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FDA 510(k), K930348, COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM
FDA 510(k), K930348, COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM
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510(K) Number: K930348
Device Name: COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM
Manufacturer: BOSTON SCIENTIFIC CORP.
Device Classification Name: Endoscopic Cytology Brush
Regulation Number: 876.1500
Classification Product Code: FDX
Date Received: 01/25/1993
Decision Date: 09/03/1993
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM
Manufacturer: BOSTON SCIENTIFIC CORP.
Device Classification Name: Endoscopic Cytology Brush
Regulation Number: 876.1500
Classification Product Code: FDX
Date Received: 01/25/1993
Decision Date: 09/03/1993
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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