510(k) K170743
K170743 is an FDA 510(k) premarket notification submitted by AngioDynamics, Inc. for the device "AngioDynamics Total Abscession Biliary Drainage Catheter". The FDA issued a decision of Substantially Equivalent on Mar 30, 2017. The device falls under product code FGE (Stents, Drains And Dilators For The Biliary Ducts), a Class II device regulated under 21 CFR 876.5010. AngioDynamics, Inc. has 89 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 30, 2017
- Date Received
- Mar 10, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stents, Drains And Dilators For The Biliary Ducts
- Device Class
- Class II
- Regulation Number
- 876.5010
- Review Panel
- GU
- Submission Type
- 510(k)