The following data is part of a premarket notification filed by Itl Corporation Pty, Ltd with the FDA for Blood Bank Supplies.
| Device ID | BK170102 |
| 510k Number | BK170102 |
| Device Name: | Blood Bank Supplies |
| Classification | Supplies, Blood-bank |
| Applicant | ITL Corporation Pty, Ltd 41-45 Tennant Street Canberra Act 2609, AS |
| 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 | 2017-09-01 |
| Decision Date | 2017-11-28 |