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FRESENIUS MODIFIED F400 LOW VOLUME HEMOCONCENTRATOR F3000 & MODIFIED F400 LOW VOL HEMOCONCENTRATOR W/TUBING SET F3000TS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992275
510(k) Type
Special
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1999
Days to Decision
28 days
Submission Type
Summary

FRESENIUS MODIFIED F400 LOW VOLUME HEMOCONCENTRATOR F3000 & MODIFIED F400 LOW VOL HEMOCONCENTRATOR W/TUBING SET F3000TS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992275
510(k) Type
Special
Applicant
FRESENIUS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1999
Days to Decision
28 days
Submission Type
Summary