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HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY

Page Type
Cleared 510(K)
510(k) Number
K930235
510(k) Type
Traditional
Applicant
TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1993
Days to Decision
240 days
Submission Type
Statement

HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY

Page Type
Cleared 510(K)
510(k) Number
K930235
510(k) Type
Traditional
Applicant
TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1993
Days to Decision
240 days
Submission Type
Statement