Last synced on 25 November 2022 at 11:04 pm

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