Last synced on 30 May 2025 at 11:05 pm

HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923593
510(k) Type
Traditional
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1992
Days to Decision
64 days
Submission Type
Statement

HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923593
510(k) Type
Traditional
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1992
Days to Decision
64 days
Submission Type
Statement