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FIBRINOGEN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K915462
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
91 days
Submission Type
Statement

FIBRINOGEN CONTROL

Page Type
Cleared 510(K)
510(k) Number
K915462
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
91 days
Submission Type
Statement