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LIQUID FIBRINOGEN FDP CONTROL LEVEL 1 & 2

Page Type
Cleared 510(K)
510(k) Number
K934741
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1994
Days to Decision
342 days
Submission Type
Statement

LIQUID FIBRINOGEN FDP CONTROL LEVEL 1 & 2

Page Type
Cleared 510(K)
510(k) Number
K934741
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1994
Days to Decision
342 days
Submission Type
Statement