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FDA 510(k), K070129, SONOTIP II ULTRASOUND NEEDLE SYSTEM
FDA 510(k), K070129, SONOTIP II ULTRASOUND NEEDLE SYSTEM
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510(K) Number: K070129
Device Name: SONOTIP II ULTRASOUND NEEDLE SYSTEM
Manufacturer: MEDI-GLOBE CORPORATION
Device Classification Name: biopsy needle
Regulation Number: 876.1075
Classification Product Code: FCG
Date Received: 01/16/2007
Decision Date: 01/31/2007
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: SONOTIP II ULTRASOUND NEEDLE SYSTEM
Manufacturer: MEDI-GLOBE CORPORATION
Device Classification Name: biopsy needle
Regulation Number: 876.1075
Classification Product Code: FCG
Date Received: 01/16/2007
Decision Date: 01/31/2007
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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