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HEMOSIL FIBRINOGEN-C

Page Type
Cleared 510(K)
510(k) Number
K073367
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2007
Days to Decision
27 days
Submission Type
Summary

HEMOSIL FIBRINOGEN-C

Page Type
Cleared 510(K)
510(k) Number
K073367
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2007
Days to Decision
27 days
Submission Type
Summary