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TRANSONIC HEMODIALYSIS MONITOR, CARDIAC OUTPUT, MODEL HD01-CO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980906
510(k) Type
Traditional
Applicant
TRANSONIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1998
Days to Decision
210 days
Submission Type
Summary

TRANSONIC HEMODIALYSIS MONITOR, CARDIAC OUTPUT, MODEL HD01-CO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980906
510(k) Type
Traditional
Applicant
TRANSONIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1998
Days to Decision
210 days
Submission Type
Summary