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VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962700
510(k) Type
Traditional
Applicant
Vasamedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1997
Days to Decision
271 days
Submission Type
Summary

VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962700
510(k) Type
Traditional
Applicant
Vasamedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1997
Days to Decision
271 days
Submission Type
Summary