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FIBRINOGEN ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K896052
510(k) Type
Traditional
Applicant
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1989
Days to Decision
22 days

FIBRINOGEN ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K896052
510(k) Type
Traditional
Applicant
MEDICAL DIAGNOSTIC TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/1989
Days to Decision
22 days