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Heraeus-Christ GmbH
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K840768
CENTRIFUGES
May 7, 1984
K840767
HAEMOFUGE A. BIOFUGE A. & B
April 17, 1984