The following data is part of a premarket notification filed by Cobe Cardiovascular, Inc. with the FDA for Standard Volume Processing Set For The Cobe Brat 2 Autologous Blood Salvage System.
Device ID | K973627 |
510k Number | K973627 |
Device Name: | STANDARD VOLUME PROCESSING SET FOR THE COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM |
Classification | Apparatus, Autotransfusion |
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 | CAC |
CFR Regulation Number | 868.5830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-24 |
Decision Date | 1997-11-03 |
Summary: | summary |