The following data is part of a premarket notification filed by Helmer Labs., Inc. with the FDA for Blood Bank Supplies.
| Device ID | BK850018 |
| 510k Number | BK850018 |
| Device Name: | Blood Bank Supplies |
| Classification | Supplies, Blood-bank |
| Applicant | Helmer Labs., Inc. 5415 Distribution Drive Fort Wayne, IN 46825 |
| 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 | 1985-08-27 |
| Decision Date | 1985-10-21 |