Last synced on 18 July 2025 at 11:06 pm

HEMOCHRON CONTROL ACT TEST TUBE NORMAL/ABNOR. I/II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882481
510(k) Type
Traditional
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1988
Days to Decision
75 days

HEMOCHRON CONTROL ACT TEST TUBE NORMAL/ABNOR. I/II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882481
510(k) Type
Traditional
Applicant
INTERNATIONAL TECHNIDYNE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1988
Days to Decision
75 days