The following data is part of a premarket notification filed by Dia Tech with the FDA for Centrifuge, Cell-washing, Automated For Immunohematology.
| Device ID | BK830025 |
| 510k Number | BK830025 |
| Device Name: | Centrifuge, Cell-Washing, Automated For Immunohematology |
| Classification | Centrifuge, Cell-washing, Automated For Immuno-hematology |
| Applicant | Dia Tech 2525 Shader Road Orlando, FL 328 |
| Product Code | KSN |
| CFR Regulation Number | 864.9285 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-09 |
| Decision Date | 1984-01-10 |