The following data is part of a premarket notification filed by Fresenius Usa/seratronics Inc. with the FDA for Blood And Plasma Warming Devices.
| Device ID | BK880018 |
| 510k Number | BK880018 |
| Device Name: | Blood And Plasma Warming Devices |
| Classification | Device, Warming. Blood And Plasma |
| Applicant | Fresenius USA/Seratronics Inc. 4090 Pike Lane Concord, CA 94502 |
| Product Code | KZL |
| CFR Regulation Number | 864.9205 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-06-30 |
| Decision Date | 1988-08-25 |