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CENTRIFIQ BLOOD CONTROL

Page Type
Cleared 510(K)
510(k) Number
K935343
510(k) Type
Traditional
Applicant
HEMATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1994
Days to Decision
128 days
Submission Type
Statement

CENTRIFIQ BLOOD CONTROL

Page Type
Cleared 510(K)
510(k) Number
K935343
510(k) Type
Traditional
Applicant
HEMATRONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1994
Days to Decision
128 days
Submission Type
Statement