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FDA 510(k), K070475, MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
FDA 510(k), K070475, MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
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510(K) Number: K070475
Device Name: MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
Manufacturer: GIVEN IMAGING LTD.
Device Classification Name: system, imaging, gastrointestinal, wireless, capsule
Regulation Number: 876.1300
Classification Product Code: NEZ
Date Received: 02/20/2007
Decision Date: 05/07/2007
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
Manufacturer: GIVEN IMAGING LTD.
Device Classification Name: system, imaging, gastrointestinal, wireless, capsule
Regulation Number: 876.1300
Classification Product Code: NEZ
Date Received: 02/20/2007
Decision Date: 05/07/2007
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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