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

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