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HEMOTEC ACT I SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843459
510(k) Type
Traditional
Applicant
HEMOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1984
Days to Decision
98 days

HEMOTEC ACT I SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843459
510(k) Type
Traditional
Applicant
HEMOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1984
Days to Decision
98 days