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FRESENIUS BLOOD VOLUME MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982926
510(k) Type
Traditional
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1999
Days to Decision
379 days
Submission Type
Summary

FRESENIUS BLOOD VOLUME MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982926
510(k) Type
Traditional
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1999
Days to Decision
379 days
Submission Type
Summary