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FRESENIUS HEMOFLOW F60 AND F80

Page Type
Cleared 510(K)
510(k) Number
K870724
510(k) Type
Traditional
Applicant
SERATRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1987
Days to Decision
36 days

FRESENIUS HEMOFLOW F60 AND F80

Page Type
Cleared 510(K)
510(k) Number
K870724
510(k) Type
Traditional
Applicant
SERATRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1987
Days to Decision
36 days