The following data is part of a premarket notification filed by Cobe Laboratories, Inc. with the FDA for Automated Blood Cell Separators.
| Device ID | BK900002 |
| 510k Number | BK900002 |
| Device Name: | Automated Blood Cell Separators |
| Classification | Separator, Automated, Blood Cell, Diagnostic |
| Applicant | Cobe Laboratories, Inc. 1185 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 | 1990-01-03 |
| Decision Date | 1990-06-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 35020583705006 | BK900002 | 0 |
| 05020583705005 | BK900002 | 0 |