The following data is part of a premarket notification filed by Cobe Cardiovascular, Inc. with the FDA for Automated Blood Cell Separators.
| Device ID | BK990025 |
| 510k Number | BK990025 |
| Device Name: | Automated Blood Cell Separators |
| Classification | Separator, Automated, Blood Cell, Diagnostic |
| Applicant | COBE Cardiovascular, Inc. 1201 Oak Street Lakewood, CO 80215 |
| Product Code | GKT |
| CFR Regulation Number | 864.9245 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-31 |
| Decision Date | 2000-04-07 |