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FIBRINOGEN FDP CONTROL

Page Type
Cleared 510(K)
510(k) Number
K915503
510(k) Type
Traditional
Applicant
CALA DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
52 days
Submission Type
Statement

FIBRINOGEN FDP CONTROL

Page Type
Cleared 510(K)
510(k) Number
K915503
510(k) Type
Traditional
Applicant
CALA DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
52 days
Submission Type
Statement