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CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042850
510(k) Type
Traditional
Applicant
STEREOTAXIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2006
Days to Decision
663 days
Submission Type
Summary

CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042850
510(k) Type
Traditional
Applicant
STEREOTAXIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2006
Days to Decision
663 days
Submission Type
Summary