The following data is part of a premarket notification filed by Sarstedt, Inc. with the FDA for Blood Mixing And Weighing Devices.
| Device ID | BK030006 |
| 510k Number | BK030006 |
| Device Name: | Blood Mixing And Weighing Devices |
| Classification | Device, Blood Mixing And Blood Weighing |
| Applicant | Sarstedt, Inc. 1025 Saint James Church Rd. Newton, NC 20865 US |
| Product Code | KSQ |
| CFR Regulation Number | 864.9195 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Abbrevia |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-02-04 |
| Decision Date | 2003-02-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04028339620139 | BK030006 | 0 |