The following data is part of a premarket notification filed by Bio-rad Medical Diagnostics Gmbh with the FDA for Quality Control Kits For Blood Banking Reagents.
Pre-market Notification Details
Device ID
BK170075
510k Number
BK170075
Device Name:
Quality Control Kits For Blood Banking Reagents
Classification
Kit, Quality Control For Blood Banking Reagents
Applicant
Bio-Rad Medical Diagnostics GmbH industriestrasse 1 Dreieich, 63303, GM