510(k) K002130
K002130 is an FDA 510(k) premarket notification submitted by Medinol, Ltd. for the device "NIR BILIARY STENT". The FDA issued a decision of Substantially Equivalent - With Limitations on Oct 30, 2000. 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. Medinol, Ltd. has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESU (Substantially Equivalent - With Limitations)
- Decision Date
- Oct 30, 2000
- Date Received
- Jul 14, 2000
- 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)