The following data is part of a premarket notification filed by Terumo Corporation with the FDA for Transfer Sets.
| Device ID | BK890032 |
| 510k Number | BK890032 |
| Device Name: | Transfer Sets |
| Classification | Set, Transfer (blood/plasma) |
| Applicant | Terumo Corporation 125 Blue Ball Road Elkton, MD 21921 |
| Product Code | KSB |
| CFR Regulation Number | 864.9875 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-30 |
| Decision Date | 1990-07-18 |