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 |