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FRESENIUS BLOOD VOLUME MONITOR

Page Type
Cleared 510(K)
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)
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