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24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012143
510(k) Type
Special
Applicant
Medtronic Cardiac Surgical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
106 days
Submission Type
Summary

24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012143
510(k) Type
Special
Applicant
Medtronic Cardiac Surgical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2001
Days to Decision
106 days
Submission Type
Summary