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COULTER BODY FLUID CONTROL

Page Type
Cleared 510(K)
510(k) Number
K082162
510(k) Type
Traditional
Applicant
BECKMAN COULTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2009
Days to Decision
187 days
Submission Type
Summary

COULTER BODY FLUID CONTROL

Page Type
Cleared 510(K)
510(k) Number
K082162
510(k) Type
Traditional
Applicant
BECKMAN COULTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2009
Days to Decision
187 days
Submission Type
Summary