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AGILIS NXT STEERABLE INTRODUCER, MODEL G408324

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081645
510(k) Type
Special
Applicant
ST. JUDE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2008
Days to Decision
180 days
Submission Type
Summary

AGILIS NXT STEERABLE INTRODUCER, MODEL G408324

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081645
510(k) Type
Special
Applicant
ST. JUDE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2008
Days to Decision
180 days
Submission Type
Summary