The following data is part of a premarket notification filed by Biomerieux, Inc. with the FDA for Bacterial Detection Systems For Platelet Transfusion Products.
Device ID | BK170142 |
510k Number | BK170142 |
Device Name: | Bacterial Detection Systems For Platelet Transfusion Products |
Classification | System, Detection, Bacterial, For Platelet Transfusion Products |
Applicant | bioMerieux, Inc. 595 Anglum Road Hazelwood, MO 63042 US |
Product Code | MZC |
CFR Regulation Number | 866.2560 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Traditio |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-03 |
Decision Date | 2018-02-01 |