The following data is part of a premarket notification filed by Genetic Testing Institute with the FDA for Blood Bank Supplies.
| Device ID | BK930014 |
| 510k Number | BK930014 |
| Device Name: | Blood Bank Supplies |
| Classification | Supplies, Blood-bank |
| Applicant | Genetic Testing Institute 1701 W. Wisconsin Avenue, Suite 429 Milwaukee, WI 53233 |
| Product Code | KSS |
| CFR Regulation Number | 864.9050 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-04-23 |
| Decision Date | 1993-10-28 |