The following data is part of a premarket notification filed by Dupaco with the FDA for Device, Warming, Blood And Plasma.
| Device ID | BK950019 |
| 510k Number | BK950019 |
| Device Name: | Device, Warming, Blood And Plasma |
| Classification | Device, Warming. Blood And Plasma |
| Applicant | DUPACO 2620 Temple Heights Dr. Oceanside, CA 92056 |
| 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 | 1995-03-06 |
| Decision Date | 1995-04-27 |