The following data is part of a premarket notification filed by Olympus Medical Systems Corporation with the FDA for Xchf-t160 Videoscope.
Device ID | K082576 |
510k Number | K082576 |
Device Name: | XCHF-T160 VIDEOSCOPE |
Classification | Choledochoscope And Accessories, Flexible/rigid |
Applicant | OLYMPUS MEDICAL SYSTEMS CORPORATION 3500 CORPORATE PARKWAY PO BOX 610 Center Valley, PA 18034 -0610 |
Contact | Stacy A Kluesner |
Correspondent | Stacy A Kluesner OLYMPUS MEDICAL SYSTEMS CORPORATION 3500 CORPORATE PARKWAY PO BOX 610 Center Valley, PA 18034 -0610 |
Product Code | FBN |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-05 |
Decision Date | 2008-10-21 |
Summary: | summary |