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GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024071
510(k) Type
Special
Applicant
GUIDANT CORPORATION, CARDIAC SURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2003
Days to Decision
66 days
Submission Type
Summary

GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024071
510(k) Type
Special
Applicant
GUIDANT CORPORATION, CARDIAC SURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2003
Days to Decision
66 days
Submission Type
Summary