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MODIFIED HOLLOW FIBERS USED IN DIAFILTER HEMOFIL.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873887
510(k) Type
Traditional
Applicant
W.R. GRACE & CO.-CONN.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1987
Days to Decision
77 days

MODIFIED HOLLOW FIBERS USED IN DIAFILTER HEMOFIL.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873887
510(k) Type
Traditional
Applicant
W.R. GRACE & CO.-CONN.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1987
Days to Decision
77 days