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PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013120
510(k) Type
Traditional
Applicant
MEDAMICUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2002
Days to Decision
128 days
Submission Type
Summary

PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013120
510(k) Type
Traditional
Applicant
MEDAMICUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2002
Days to Decision
128 days
Submission Type
Summary