510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
Manual Blood Grouping And Antibody Test Systems
Bio-Rad Medical Diagnostics GmbH
The following data is part of a premarket notification filed by Bio-rad Medical Diagnostics Gmbh with the FDA for 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.s. Food & Drug Administration Follow Fda En Español Search Fda Home Food Drugs Medical Devices .
Pre-market Notification Details
Device ID
BK170065
510k Number
BK170065
Device Name:
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
Classification
Manual Blood Grouping And Antibody Test Systems
Applicant
Bio-Rad Medical Diagnostics GmbH industriestrasse 1 Dreieich, 63303, GM