• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K150692, AXIOS Stent with Electrocautery Enhanced Delivery System, by Boston Scientific Corp

FDA 510(k) K150692, AXIOS Stent with Electrocautery Enhanced Delivery System, by Boston Scientific Corp

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510(K) Number: K150692
Device Name: AXIOS Stent with Electrocautery Enhanced Delivery System
Manufacturer: Boston Scientific Corp
Device Classification Name: pancreatic stent, covered, metallic, removable
Regulation Number: 876.5015
Classification Product Code: PCU
Date Received: 03/18/2015
Decision Date: 08/05/2015
Regulation Medical Specialty: Gastroenterology/Urology
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