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 |