The following data is part of a premarket notification filed by Biomet Biologics, Inc. with the FDA for Blood Bank Supplies.
| Device ID | BK070003 |
| 510k Number | BK070003 |
| Device Name: | Blood Bank Supplies |
| Classification | Supplies, Blood-bank |
| Applicant | Biomet Biologics, Inc. 56 East Bell Drive po Box 587 Warsaw, IN 46581 US |
| Product Code | KSS |
| CFR Regulation Number | 864.9050 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-02 |
| Decision Date | 2007-02-22 |