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Ion™ Endoluminal System (Ion™ Fully Articulating Catheter) (IF1000)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240135
510(k) Type
Traditional
Applicant
Intuitive Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2024
Days to Decision
76 days
Submission Type
Summary

Ion™ Endoluminal System (Ion™ Fully Articulating Catheter) (IF1000)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240135
510(k) Type
Traditional
Applicant
Intuitive Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2024
Days to Decision
76 days
Submission Type
Summary