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FRESENIUS HEMOFLOW F6 AND F8

Page Type
Cleared 510(K)
510(k) Number
K870725
510(k) Type
Traditional
Applicant
SERATRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1987
Days to Decision
66 days

FRESENIUS HEMOFLOW F6 AND F8

Page Type
Cleared 510(K)
510(k) Number
K870725
510(k) Type
Traditional
Applicant
SERATRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1987
Days to Decision
66 days