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FDA 510(k), K121370, VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE
FDA 510(k), K121370, VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE
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510(K) Number: K121370
Device Name: VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE
Manufacturer: VECTEC
Device Classification Name: pneumoperitoneum needle
Regulation Number: 876.1500
Classification Product Code: FHO
Date Received: 05/07/2012
Decision Date: 08/02/2013
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: VECTEC DISPOSABLE PNEUMOPERITONEUM NEEDLE
Manufacturer: VECTEC
Device Classification Name: pneumoperitoneum needle
Regulation Number: 876.1500
Classification Product Code: FHO
Date Received: 05/07/2012
Decision Date: 08/02/2013
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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