The following data is part of a premarket notification filed by Cobe Cardiovascular, Inc. with the FDA for Cobe Closed Venous Reservoir Bags With Smarx T, Models Vrb 1200 And Vrb 1800.
Device ID | K980786 |
510k Number | K980786 |
Device Name: | COBE CLOSED VENOUS RESERVOIR BAGS WITH SMARX T, MODELS VRB 1200 AND VRB 1800 |
Classification | Reservoir, Blood, Cardiopulmonary Bypass |
Applicant | COBE CARDIOVASCULAR, INC. 14401 WEST 65TH WAY Arvada, CO 80004 |
Contact | Lynne Leonard |
Correspondent | Lynne Leonard COBE CARDIOVASCULAR, INC. 14401 WEST 65TH WAY Arvada, CO 80004 |
Product Code | DTN |
CFR Regulation Number | 870.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-03-02 |
Decision Date | 1998-08-24 |
Summary: | summary |