The following data is part of a premarket notification filed by Mallinckrodt Medical, Inc. with the FDA for Blood And Plasma Warming Devices.
Device ID | BK960075 |
510k Number | BK960075 |
Device Name: | Blood And Plasma Warming Devices |
Classification | Device, Warming. Blood And Plasma |
Applicant | Mallinckrodt Medical, Inc. 675 Mcdonnell Boulevard St. Louis, MO 63134 |
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 | 1996-10-15 |
Decision Date | 1997-02-28 |