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HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930068
510(k) Type
Traditional
Applicant
TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1993
Days to Decision
239 days
Submission Type
Statement

HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930068
510(k) Type
Traditional
Applicant
TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1993
Days to Decision
239 days
Submission Type
Statement