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FDA 510(k) Applications Submitted by BENITA BOURQUE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K955016
11/02/1995
4C PLUS COULTER CELL CONTROL
COULTER CORP.
K955334
11/20/1995
COULTER LINEARITY CONTROL
COULTER CORP.
K970253
01/22/1997
COBE CENTRYSYSTEM 3 DIALYSIS CONTROL UNIT/COBE CARTRIDGE BLOOD TUBING SET
GAMBRO HEALTHCARE
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