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N-ASSAY TIA FIBRINOGEN TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K965113
510(k) Type
Traditional
Applicant
Crestat Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1997
Days to Decision
117 days
Submission Type
Statement

N-ASSAY TIA FIBRINOGEN TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K965113
510(k) Type
Traditional
Applicant
Crestat Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1997
Days to Decision
117 days
Submission Type
Statement