The following data is part of a premarket notification filed by Olympus Medical Systems Corporation with the FDA for Single Use Biliary Drainage Stent V.
| Device ID | K103478 |
| 510k Number | K103478 |
| Device Name: | SINGLE USE BILIARY DRAINAGE STENT V |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | OLYMPUS MEDICAL SYSTEMS CORPORATION 3500 CORPORATE PARKWAY PO BOX 610 Center Valley, PA 18034 -0610 |
| Contact | Stacy Abbatiello Kluesner |
| Correspondent | Stacy Abbatiello Kluesner OLYMPUS MEDICAL SYSTEMS CORPORATION 3500 CORPORATE PARKWAY PO BOX 610 Center Valley, PA 18034 -0610 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-11-26 |
| Decision Date | 2011-02-24 |
| Summary: | summary |