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subpart-f—cardiovascular-therapeutic-devices/

HEMOTEC HEPCON/SYSTEM FOUR & FOUR P

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K820410
510(k) Type: Traditional
Applicant: HEMOTEC, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/9/1982
Days to Decision: 56 days

FDA Browser

subpart-f—cardiovascular-therapeutic-devices/

HEMOTEC HEPCON/SYSTEM FOUR & FOUR P

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K820410
510(k) Type: Traditional
Applicant: HEMOTEC, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/9/1982
Days to Decision: 56 days