510(k) K955110
K955110 is an FDA 510(k) premarket notification submitted by Navarre Biomedical , Ltd. for the device "NAVARRE PERCUTANEOUS BILIARY DRAINAGE". The FDA issued a decision of Substantially Equivalent on November 7, 1996. 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. Navarre Biomedical , Ltd. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 7, 1996
- Date Received
- November 8, 1995
- Clearance Type
- Traditional
- 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