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FRESENIUS HEMOFLOW, F40M, F50M, F60M & F80M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892262
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1989
Days to Decision
20 days

FRESENIUS HEMOFLOW, F40M, F50M, F60M & F80M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892262
510(k) Type
Traditional
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1989
Days to Decision
20 days